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CROMOLYN SODIUM solution


  1. Description
  2. Clinical Pharmacology
  3. Clinical Studies
  4. Indications And Usage
  5. Contraindications
  6. Warnings
  7. Precautions
  8. Adverse Reactions
  9. Dosage And Administration
  10. How Supplied
  11. Patient Instructions
  12. Principal Display Panel
  13. Description
  14. Clinical Pharmacology
  15. Indications And Usage
  16. Contraindications
  17. Warnings
  18. Precautions
  19. Adverse Reactions
  20. Overdosage
  21. Dosage And Administration
  22. How Supplied
  23. Living A Full Life With Asthma
  24. Package/label Display Panel, Part 2 Of 2
  25. Living A Full Life With Asthma

Description  

Each 5 mL ampule of Cromolyn Sodium, USP contains 100 mg cromolyn sodium, USP, in purified water. Cromolyn sodium is a hygroscopic, white powder having little odor. It may leave a slightly bitter aftertaste. Cromolyn Sodium, USP Oral Concentrate is clear, colorless, and sterile. It is intended for oral use.

Chemically, cromolyn sodium is disodium 5,5 -[(2-hydroxytrimethylene)dioxy]bis[4-oxo-4H-1-benzopyran-2-carboxylate]. The empirical formula is C23H14Na2O11; the molecular weight is 512.34. Its chemical structure is:

Cromolyn Sodium Structural Formula

Pharmacologic Category: Mast cell stabilizer

Therapeutic Category: Antiallergic

Clinical Pharmacology  

In vitro and in vivo animal studies have shown that cromolyn sodium inhibits the release of mediators from sensitized mast cells. Cromolyn sodium acts by inhibiting the release of histamine and leukotrienes (SRS-A) from the mast cell.

Cromolyn sodium has no intrinsic vasoconstrictor, antihistamine, or glucocorticoid activity.

Cromolyn sodium is poorly absorbed from the gastrointestinal tract. No more than 1% of an administered dose is absorbed by humans after oral administration, the remainder being excreted in the feces. Very little absorption of cromolyn sodium was seen after oral administration of 500 mg by mouth to each of 12 volunteers. From 0.28 to 0.50% of the administered dose was recovered in the first 24 hours of urinary excretion in 3 subjects. The mean urinary excretion of an administered dose over 24 hours in the remaining 9 subjects was 0.45%.

Clinical Studies  

Four randomized, controlled clinical trials were conducted with Cromolyn Sodium, USP in patients with either cutaneous or systemic mastocytosis; two of which utilized a placebo-controlled crossover design, one utilized an active-controlled (chlorpheniramine plus cimetidine) crossover design, and one utilized a placebo-controlled parallel group design. Due to the rare nature of this disease, only 36 patients qualified for study entry, of whom 32 were considered evaluable. Consequently, formal statistical analyses were not performed. Clinically significant improvement in gastrointestinal symptoms (diarrhea, abdominal pain) were seen in the majority of patients with some improvement also seen for cutaneous manifestations (urticaria, pruritus, flushing) and cognitive function.

The benefit seen with Cromolyn Sodium, USP 200 mg QID was similar to chlorpheniramine (4 mg QID) plus cimetidine (300 mg QID) for both cutaneous and systemic symptoms of mastocytosis.

Clinical improvement occurred within 2-6 weeks of treatment initiation and persisted for 2-3 weeks after treatment withdrawal. Cromolyn Sodium, USP did not affect urinary histamine levels or peripheral eosinophilia, although neither of these variables appeared to correlate with disease severity. Positive clinical benefits were also reported for 37 of 51 patients who received Cromolyn Sodium, USP in United States and foreign humanitarian programs.

Indications And Usage  

Cromolyn Sodium, USP is indicated in the management of patients with mastocytosis. Use of this product has been associated with improvement in diarrhea, flushing, headaches, vomiting, urticaria, abdominal pain, nausea, and itching in some patients.

Contraindications  

Cromolyn Sodium, USP is contraindicated in those patients who have shown hypersensitivity to cromolyn sodium.

Warnings  

The recommended dosage should be decreased in patients with decreased renal or hepatic function. Severe anaphylactic reactions may occur rarely in association with cromolyn sodium administration.

Precautions  

In view of the biliary and renal routes of excretion of Cromolyn Sodium, USP, consideration should be given to decreasing the dosage of the drug in patients with impaired renal or hepatic function.

Carcinogenesis, Mutagenesis, Impairment of Fertility

In carcinogenicity studies in mice, hamsters, and rats, cromolyn sodium had no neoplastic effects at intraperitoneal doses up to 150 mg/kg three days per week for 12 months in mice, at intraperitoneal doses up to 53 mg/kg three days per week for 15 weeks followed by 17.5 mg/kg three days per week for 37 weeks in hamsters, and at subcutaneous doses up to 75 mg/kg six days per week for 18 months in rats. These doses in mice, hamsters, and rats are less than the maximum recommended daily oral dose in adults and children on a mg/m2 basis.

Cromolyn sodium showed no mutagenic potential in Ames Salmonella/microsome plate assays, mitotic gene conversion in Saccharomyces cerevisiae and in an in vitro cytogenetic study in human peripheral lymphocytes.

In rats, cromolyn sodium showed no evidence of impaired fertility at subcutaneous doses up to 175 mg/kg in males (approximately equal to the maximum recommended daily oral dose in adults on a mg/m2 basis) and 100 mg/kg in females (less than the maximum recommended daily oral dose in adults on a mg/m2 basis).

Pregnancy

In reproductive studies in pregnant mice, rats, and rabbits, cromolyn sodium produced no evidence of fetal malformations at subcutaneous doses up to 540 mg/kg in mice (approximately equal to the maximum recommended daily oral dose in adults on a mg/m2 basis) and 164 mg/kg in rats (less than the maximum recommended daily oral dose in adults on a mg/m2 basis) or at intravenous doses up to 485 mg/kg in rabbits (approximately 4 times the maximum recommended daily oral dose in adults on a mg/m2 basis). There are, however, no adequate and well controlled studies in pregnant women.

Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Drug Interaction During Pregnancy

In pregnant mice, cromolyn sodium alone did not cause significant increases in resorptions or major malformations at subcutaneous doses up to 540 mg/kg (approximately equal to the maximum recommended daily oral dose in adults on a mg/m2 basis). Isoproterenol alone increased both resorptions and major malformations (primarily cleft palate) at a subcutaneous dose of 2.7 mg/kg (approximately 7 times the maximum recommended daily inhalation dose in adults on a mg/m2 basis). The incidence of major malformations increased further when cromolyn sodium at a subcutaneous dose of 540 mg/kg was added to isoproterenol at a subcutaneous dose of 2.7 mg/kg. No such interaction was observed in rats or rabbits.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Cromolyn Sodium, USP is administered to a nursing woman.

Pediatric Use

In adult rats no adverse effects of cromolyn sodium were observed at oral doses up to 6144 mg/kg (approximately 25 times the maximum recommended daily oral dose in adults on a mg/m2 basis). In neonatal rats, cromolyn sodium increased mortality at oral doses of 1000 mg/kg or greater (approximately 9 times the maximum recommended daily oral dose in infants on a mg/m2 basis) but not at doses of 300 mg/kg or less (approximately 3 times the maximum recommended daily oral dose in infants on a mg/m2 basis). Plasma and kidney concentrations of cromolyn after oral administration to neonatal rats were up to 20 times greater than those in older rats. In term infants up to six months of age, available clinical data suggest that the dose should not exceed 20 mg/kg/day. The use of this product in pediatric patients less than two years of age should be reserved for patients with severe disease in which the potential benefits clearly outweigh the risks.

Geriatric Use

Clinical studies of Cromolyn Sodium, USP did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

Adverse Reactions  

Most of the adverse events reported in mastocytosis patients have been transient and could represent symptoms of the disease. The most frequently reported adverse events in mastocytosis patients who have received Cromolyn Sodium, USP during clinical studies were headache and diarrhea, each of which occurred in 4 of the 87 patients. Pruritus, nausea, and myalgia were each reported in 3 patients and abdominal pain, rash, and irritability in 2 patients each. One report of malaise was also recorded.

To report SUSPECTED ADVERSE REACTIONS, contact Wallace Pharmaceuticals Inc. at 1-877-999-8407 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Other Adverse Events: Additional adverse events have been reported during studies in other clinical conditions and from worldwide postmarketing experience. In most cases the available information is incomplete and attribution to the drug cannot be determined. The majority of these reports involve the gastrointestinal system and include: diarrhea, nausea, abdominal pain, constipation, dyspepsia, flatulence, glossitis, stomatitis, vomiting, dysphagia, esophagospasm.

Other less commonly reported events (the majority representing only a single report) include the following:

Skin: pruritus, rash, urticaria/angioedema, erythema/ burning, photosensitivity

Musculoskeletal: arthralgia, myalgia, stiffness/weakness of legs

Neurologic: headache, dizziness, hypoesthesia, paresthesia, migraine, convulsions, flushing

Psychiatric: psychosis, anxiety, depression, hallucinations, behavior change, insomnia, nervousness

Heart Rate: tachycardia, premature ventricular contractions (PVCs), palpitations

Respiratory: pharyngitis, dyspnea

Miscellaneous: fatigue, edema, unpleasant taste, chest pain, postprandial lightheadedness and lethargy, dysuria, urinary frequency, purpura, hepatic function test abnormal, polycythemia, neutropenia, pancytopenia, tinnitus, lupus erythematosus (LE) syndrome

Dosage And Administration  

NOT FOR INHALATION OR INJECTION. SEE DIRECTIONS FOR USE.

The usual starting dose is as follows:

Adults and Adolescents (13 Years and Older)

Two ampules four times daily, taken one-half hour before meals and at bedtime.

Children 2-12 Years

One ampule four times daily, taken one-half hour before meals and at bedtime.

Pediatric Patients Under 2 Years

Not recommended.

If satisfactory control of symptoms is not achieved within two to three weeks, the dosage may be increased but should not exceed 40 mg/kg/day.

Patients should be advised that the effect of Cromolyn Sodium, USP therapy is dependent upon its administration at regular intervals, as directed.

Maintenance Dose

Once a therapeutic response has been achieved, the dose may be reduced to the minimum required to maintain the patient with a lower degree of symptomatology. To prevent relapses, the dosage should be maintained.

Administration

Cromolyn Sodium, USP should be administered as a solution at least 1/2 hour before meals and at bedtime after preparation according to the following directions:

1.
Break open ampule(s) and squeeze liquid contents of ampule(s) into a glass of water.
2.
Stir solution.
3.
Drink all of the liquid.

How Supplied  

Cromolyn Sodium, USP Oral Concentrate is an unpreserved, colorless solution supplied in a low density polyethylene plastic unit dose ampule with 8 ampules per foil pouch. Each 5 mL ampule contains 100 mg cromolyn sodium, USP, in purified water.

NDC 51525-0470-8 8 ampules x 5 mL

NDC 51525-0470-9 96 ampules x 5 mL

Cromolyn Sodium, USP Oral Concentrate should be stored between 15 -30 C (59 -86 F) and protected from light. Do not use if it contains a precipitate or becomes discolored. Keep out of the reach of children.

Store ampules in foil pouch until ready for use.

Distributed by:
Wallace Pharmaceuticals Inc.
Somerset, New Jersey 08873-4120
Wallace and Wallace Logo are registered trademarks of Wallace Pharmaceuticals Inc., a Mylan company
2018 Mylan Specialty LP

Rev. 10/2018
STW-PRS7096-642R02
IN-0470-03

Patient Instructions  

Cromolyn Sodium, USP
Oral Concentrate

For Oral Use Only Not for Inhalation or Injection.

How to Use Cromolyn Sodium, USP:
As with all prescription drugs, follow the directions for dosage that your physician recommends.

The effect of Cromolyn Sodium, USP therapy is dependent upon its administration at REGULAR intervals, for as long as recommended by your physician.

Usual Starting Dose:
Adults and Adolescents (13 Years and Older):
Two ampules four times daily, taken one-half hour before meals and at bedtime.

Children 2-12 Years:
One ampule four times daily, taken one-half hour before meals and at bedtime.

Note:
Your physician may decide to increase OR decrease your dosage to achieve optimum results with Cromolyn Sodium, USP. However, do not change your dose or stop taking Cromolyn Sodium, USP without first consulting your physician.

Care & Storage:
Cromolyn Sodium, USP Oral Concentrate should be stored between 15 -30 C (59 -86 F) and protected from light. Do not use if it contains a precipitate (particles or cloudiness) or becomes discolored. Keep out of the reach of children.

Store ampules in foil pouch until ready for use.

Recycling Information: Cromolyn Sodium, USP Oral Concentrate ampules are made with a low density polyethylene plastic (recycling material code: Recycling Material Code Image LDPE).

Directions for Use:

1.Open foil pouch by tearing at serrated edge as shown.

Directions for Use Image 01

2.Remove ampule(s) from the strip.

Directions for Use Image 02

3.Open the ampule by twisting off the tabbed top section.

Directions for Use Image 03

4.Squeeze liquid contents into a glass of water. Stir solution. Drink all of the liquid. Discard the empty ampule.

Directions for Use Image 04

Distributed by:
Wallace Pharmaceuticals Inc.
Somerset, New Jersey 08873-4120

Wallace and Wallace Logo are registered trademarks of Wallace Pharmaceuticals Inc., a Mylan company
2018 Mylan Specialty LP

Rev. 10/2018
STW-ME7096-642R02
IN-0470-03

Principal Display Panel  

NDC 51525-0470-9

Cromolyn Sodium, USP
Oral Concentrate

FOR ORAL USE ONLY
NOT FOR INHALATION OR INJECTION.

Rx Only

100 mg/5 mL
96 Plastic Ampules

DESCRIPTION: Each 5 mL ampule
contains 100 mg cromolyn sodium, USP,
in purified water.

NOTE: See package circular for full
prescribing information including
contraindications, warnings and
precautions.

Cromolyn Sodium, USP Oral Concentrate should
be stored between 15 -30 C (59 -86 F)
and protected from light.
Do not use if it contains a precipitate
or becomes discolored. Keep out of
the reach of children.

Store ampules in foil pouch until ready
to use

Rev. 10/2018
STW-PRS7096-442R02
UC-0470-04

Distributed by:
Wallace Pharmaceuticals Inc.
Somerset, New Jersey 08873-4120

Wallace and Wallace Logo are registered trademarks of
Wallace Pharmaceuticals Inc., a Mylan Company

2018 Mylan Specialty LP

Cromolyn Sodium, USP Oral Concentrate Carton Label
CROMOLYN SODIUM
cromolyn sodium solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51525-0470
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CROMOLYN SODIUM (UNII: Q2WXR1I0PK) (CROMOLYN - UNII:Y0TK0FS77W) CROMOLYN SODIUM 20 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)
Product Characteristics
Color WHITE Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51525-0470-9 12 in 1 CARTON 10/21/2015
1 NDC:51525-0470-8 8 in 1 POUCH
1 5 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA authorized generic NDA020479 10/21/2015
Labeler - Wallace Pharmaceuticals Inc. (962531955)

Revised: 10/2018 Wallace Pharmaceuticals Inc.

 

For Oral Inhalation Use Only - Not for Injection

Description 

The active ingredient of cromolyn sodium inhalation solution USP is cromolyn sodium, USP. It is an inhaled anti-inflammatory agent for the preventive management of asthma. Cromolyn sodium, USP is chemically designated as disodium 5,5'- [(2-hydroxytrimethylene)dioxy] bis [4-oxo-4H-1-benzopyran-2-carboxylate]. The molecular formula is C23H14Na2O11; the molecular weight is 512.34. Cromolyn sodium, USP is a water-soluble, odorless, white, hydrated crystalline powder. It is tasteless at first, but leaves a slightly bitter aftertaste. Cromolyn sodium inhalation solution USP is clear, colorless to pale yellow, sterile and has a target pH of 5.5.

The structural formula is:

structural formula

Each 2 mL vial for oral inhalation use only contains 20 mg cromolyn sodium, USP in water for injection, USP.

Clinical Pharmacology 

In vitro and in vivo animal studies have shown that cromolyn sodium inhibits sensitized mast cell degranulation which occurs after exposure to specific antigens. Cromolyn sodium acts by inhibiting the release of mediators from mast cells. Studies show that cromolyn sodium indirectly blocks calcium ions from entering the mast cell, thereby preventing mediator release.

Cromolyn sodium inhibits both the immediate and non-immediate bronchoconstrictive reactions to inhaled antigen. Cromolyn sodium also attenuates bronchospasm caused by exercise, toluene diisocyanate, aspirin, cold air, sulfur dioxide, and environmental pollutants.

Cromolyn sodium has no intrinsic bronchodilator or antihistamine activity.

After administration by inhalation, approximately 8% of the total cromolyn sodium dose administered is absorbed and rapidly excreted unchanged, approximately equally divided between urine and bile. The remainder of the dose is either exhaled or deposited in the oropharynx, swallowed and excreted via the alimentary tract.

Indications And Usage 

Cromolyn sodium inhalation solution USP is a prophylactic agent indicated in the management of patients with bronchial asthma.

In patients whose symptoms are sufficiently frequent to require a continuous program of medication, cromolyn sodium inhalation solution USP is given by inhalation on a regular daily basis (see DOSAGE AND ADMINISTRATION). The effect of cromolyn sodium is usually evident after several weeks of treatment, although some patients show an almost immediate response.

In patients who develop acute bronchoconstriction in response to exposure to exercise, toluene diisocyanate, environmental pollutants, etc., cromolyn sodium should be given shortly before exposure to the precipitating factor (see DOSAGE AND ADMINISTRATION).

Contraindications 

Cromolyn sodium inhalation solution is contraindicated in those patients who have shown hypersensitivity to cromolyn sodium.

Warnings 

Cromolyn sodium inhalation solution has no role in the treatment of status asthmaticus.

Anaphylactic reactions with cromolyn sodium administration have been reported rarely.

Precautions 

General

Occasionally, patients may experience cough and/or bronchospasm following inhalation of cromolyn sodium. At times, patients who develop bronchospasm may not be able to continue cromolyn sodium administration despite prior bronchodilator administration. Rarely, very severe bronchospasm has been encountered.

Symptoms of asthma may recur if cromolyn sodium is reduced below the recommended dosage or discontinued.

Information for Patients

Cromolyn sodium is to be taken as directed by the physician. Because it is preventive medication, it may take up to four weeks before the patient experiences maximum benefit.

Cromolyn sodium should be used in a power-driven nebulizer with an adequate airflow rate equipped with a suitable face mask or mouthpiece.

Drug stability and safety of cromolyn sodium inhalation solution when mixed with other drugs in a nebulizer have not been established.

For additional information, see the accompanying leaflet entitled Living a Full Life with Asthma.

Carcinogenesis, Mutagenesis, and Impairment of Fertility

Long-term studies of cromolyn sodium in mice (12 months intraperitoneal administration at doses up to 150 mg/kg three days per week), hamsters (intraperitoneal administration at doses up to 53 mg/kg three days per week for 15 weeks followed by 17.5 mg/kg three days per week for 37 weeks), and rats (18 months subcutaneous treatment at doses up to 75 mg/kg six days per week) showed no neoplastic effects. These doses correspond to approximately 1.0, 0.3, and 2 times, respectively, the maximum recommended human daily inhalation dose on a mg/m2 basis.

Cromolyn sodium showed no mutagenic potential in Ames Salmonella/microsome plate assays, mitotic gene conversion in Saccharomyces cerevisiae and in an in vitro cytogenetic study in human peripheral lymphocytes.

No evidence of impaired fertility was shown in laboratory reproduction studies conducted subcutaneously in rats at the highest doses tested, 175 mg/kg/day in males and 100 mg/kg/day in females. These doses are approximately 18 and 10 times, respectively, the maximum recommended adult human daily inhalation dose on a mg/m2 basis.

Pregnancy

Teratogenic Effects

Pregnancy Category B

Reproduction studies with cromolyn sodium administered subcutaneously to pregnant mice and rats at maximum daily doses of 540 mg/kg and 164 mg/kg, respectively, and intravenously to rabbits at a maximum daily dose of 485 mg/kg produced no evidence of fetal malformations. These doses represent approximately 27, 17, and 98 times, respectively, the maximum recommended adult human daily inhalation dose on a mg/m2 basis. Adverse fetal effects (increased resorption and decreased fetal weight) were noted only at the very high parenteral doses that produced maternal toxicity. There are, however, no adequate and well-controlled studies in pregnant women.

Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Drug Interaction During Pregnancy

Cromolyn sodium and isoproterenol were studied following subcutaneous injections in pregnant mice. Cromolyn sodium alone in doses up to 540 mg/kg (approximately 27 times the maximum recommended adult human daily inhalation dose on a mg/m2 basis) did not cause significant increases in resorptions or major malformations. Isoproterenol alone at a dose of 2.7 mg/kg (approximately 7 times the maximum recommended adult human daily inhalation dose on a mg/m2 basis) increased both resorptions and malformations. The addition of cromolyn sodium (approximately 27 times the maximum recommended adult human daily inhalation dose on a mg/m2 basis) to isoproterenol (approximately 7 times the maximum recommended adult human daily inhalation dose on a mg/m2 basis) appears to have increased the incidence of both resorptions and malformations.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when cromolyn sodium is administered to a nursing woman.

Pediatric Use

Safety and effectiveness in pediatric patients below the age of 2 years have not been established.

Geriatric Use

Clinical studies of cromolyn sodium inhalation solution did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

Adverse Reactions 

Clinical experience with the use of cromolyn sodium suggests that adverse reactions are rare events. The following adverse reactions have been associated with cromolyn sodium: cough, nasal congestion, nausea, sneezing, and wheezing.

Other reactions have been reported in clinical trials; however, a causal relationship could not be established: drowsiness, nasal itching, nose bleed, nose burning, serum sickness, and stomachache.

In addition, adverse reactions have been reported with cromolyn sodium for inhalation capsules. The most common side effects are associated with inhalation of the powder and include transient cough (1 in 5 patients) and mild wheezing (1 in 25 patients). These effects rarely require treatment or discontinuation of the drug.

Information on the incidence of adverse reactions to cromolyn sodium for inhalation capsules has been derived from U.S. postmarketing surveillance experience. The following adverse reactions attributed to cromolyn sodium, based upon recurrence following readministration, have been reported in less than 1 in 10,000 patients: laryngeal edema, swollen parotid gland, angioedema, bronchospasm, joint swelling and pain, dizziness, dysuria and urinary frequency, nausea, cough, wheezing, headache, nasal congestion, rash, urticaria and lacrimation.

Other adverse reactions have been reported in less than 1 in 100,000 patients, and it is unclear whether these are attributable to the drug: anaphylaxis, nephrosis, periarteritic vasculitis, pericarditis, peripheral neuritis, pulmonary infiltrates with eosinophilia, polymyositis, exfoliative dermatitis, hemoptysis, anemia, myalgia, hoarseness, photodermatitis, and vertigo.

Overdosage 

There is no clinical syndrome associated with an overdosage of cromolyn sodium. Acute toxicity testing in a wide variety of species has demonstrated that toxicity with cromolyn sodium occurs only with very high exposure levels, regardless of whether administration was parenteral, oral or by inhalation. Parenteral administration in mice, rats, guinea pigs, hamsters, and rabbits demonstrated a median lethal dose of approximately 4000 mg/kg. Intravenous administration in monkeys also indicated a similar pattern of toxicity. The highest dose administered by the oral route in rats and mice was 8000 mg/kg, (approximately 261 and 130 times, respectively, the maximum recommended human daily inhalation dose on a mg/m2 basis) and at this dose level no deaths occurred. By inhalation, even in long term studies, it proved impossible to achieve toxic dose levels of cromolyn sodium in a range of mammalian species.

Dosage And Administration 

For management of bronchial asthma in adults and pediatric patients (two years of age and over), the usual starting dosage is the contents of one vial administered by nebulization four times a day at regular intervals.

Drug stability and safety of cromolyn sodium inhalation solution when mixed with other drugs in a nebulizer have not been established.

Patients with chronic asthma should be advised that the effect of cromolyn sodium inhalation solution therapy is dependent upon its administration at regular intervals, as directed. Cromolyn sodium inhalation solution should be introduced into the patient's therapeutic regimen when the acute episode has been controlled, the airway has been cleared and the patient is able to inhale adequately.

For the prevention of acute bronchospasm which follows exercise or exposure to cold dry air, environmental agents (e.g., animal danders, toluene diisocyanate, pollutants), etc., the usual dose is the contents of one vial administered by nebulization shortly before exposure to the precipitating factor.

It should be emphasized to the patient that the drug is poorly absorbed when swallowed and is not effective by this route of administration.

For additional information, see the accompanying leaflet entitled Living a Full Life with Asthma .

Cromolyn Sodium Inhalation Solution Therapy in Relation to Other Treatments for Asthma

Non-steroidal agents

Cromolyn sodium inhalation solution should be added to the patient's existing treatment regimen (e.g., bronchodilators). When a clinical response to cromolyn sodium inhalation solution is evident, usually within two to four weeks, and if the asthma is under good control, an attempt may be made to decrease concomitant medication usage gradually.

If concomitant medications are eliminated or required on no more than a prn basis, the frequency of administration of cromolyn sodium inhalation solution may be titrated downward to the lowest level consistent with the desired effect. The usual decrease is from four to three vials per day. It is important that the dosage be reduced gradually to avoid exacerbation of asthma. It is emphasized that in patients whose dosage has been titrated to fewer than four vials per day, an increase in the dose of cromolyn sodium inhalation solution and the introduction of, or increase in, symptomatic medications may be needed if the patient's clinical condition deteriorates.

Corticosteroids

In patients chronically receiving corticosteroids for the management of bronchial asthma, the dosage should be maintained following the introduction of cromolyn sodium inhalation solution. If the patient improves, an attempt to decrease corticosteroids should be made. Even if the corticosteroid-dependent patient fails to show symptomatic improvement following cromolyn sodium inhalation solution administration, the potential to reduce corticosteroids may nonetheless be present. Thus, gradual tapering of corticosteroid dosage may be attempted. It is important that the dose be reduced slowly, maintaining close supervision of the patient to avoid an exacerbation of asthma.

It should be borne in mind that prolonged corticosteroid therapy frequently causes an impairment in the activity of the hypothalamic-pituitary-adrenal axis and a reduction in the size of the adrenal cortex. A potentially critical degree of impairment or insufficiency may persist asymptomatically for some time even after gradual discontinuation of adrenocortical steroids. Therefore, if a patient is subjected to significant stress, such as a severe asthmatic attack, surgery, trauma or severe illness while being treated or within one year (occasionally up to two years) after corticosteroid treatment has been terminated, consideration should be given to reinstituting corticosteroid therapy. When respiratory function is impaired, as may occur in severe exacerbation of asthma, a temporary increase in the amount of corticosteroids may be required to regain control of the patient's asthma.

It is particularly important that great care be exercised if, for any reason, cromolyn sodium inhalation solution is withdrawn in cases where its use has permitted a reduction in the maintenance dose of corticosteroids. In such cases, continued close supervision of the patient is essential since there may be sudden reappearance of severe manifestations of asthma which will require immediate therapy and possible reintroduction of corticosteroids.

How Supplied 

Cromolyn Sodium Inhalation Solution USP Unit-Dose 2 mL Vial is supplied as a colorless to pale yellow solution containing 20 mg cromolyn sodium, USP, in water for injection, USP, with 5 vials per foil pouch in a carton as listed below.

60 vials per carton (NDC 0172-6406-49).

Each vial is made from a low density polyethylene (LDPE) resin.

Store at 20 to 25 C (68 to 77 F) [See USP Controlled Room Temperature]. Do not use if solution is discolored or contains a precipitate.

Retain in foil pouch until time of use.

PROTECT FROM LIGHT.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Manufactured In England By:

Norton Healthcare Limited T/A IVAX Pharmaceuticals UK

Runcorn, Cheshire WA7 3FA England

Manufactured For:

TEVA PHARMACEUTICALS USA, INC.

North Wales, PA 19454

Steri-Neb is a trademark of Norton Healthcare Limited.

Rev. A 10/2015

Living A Full Life With Asthma 

PATIENT INSTRUCTIONS

CROMOLYN SODIUM INHALATION SOLUTION USP

You or your child may be among the millions of Americans who have asthma. For most patients, asthma need not limit your lifestyle, if you closely follow the asthma management plan your doctor provides you. Your doctor has given you this instruction sheet to help you learn more about asthma and ways to control it.

WHAT IS ASTHMA?

Asthma is a disease that causes patients to have difficulty breathing. Asthma attacks occur when the air passages (airways) to the lungs close up, blocking air from passing through. The closing up is caused by two things:

  1. The muscles around the airways tighten (constrict) making the airway narrower, and
  2. The passage lining swells and produces larger amounts of mucus (a sticky liquid normally found in airways). This swelling is caused by a certain type of inflammation that can build up in the airways of patients with asthma. Inflammation and the airway sensitivity that results from it cause further attacks to occur.
airway graphic

WHAT CAUSES THESE ATTACKS?

Asthma experts know that patients with asthma have attacks because their airways are inflamed and over reactive. Their lungs become super-sensitive to certain irritants or triggers , such as cold dry air, pollen, smoke, or cat dander. In the presence of such triggers, someone with asthma may have an attack, and attacks may occur more often.

Asthma triggers fall into 6 categories:

  1. Substances that cause allergies (pollens, animal dander, molds, house dust, some foods and medicines)
  2. Infections that affect breathing (colds, flu)
  3. Emotional stress (difficult situations at home, school, or work)
  4. Strenuous exercise
  5. Irritating gases (chlorine, perfume, tobacco smoke)
  6. Sudden changes in temperature or humidity
pollen graphic

HOW TO PREVENT ASTHMA ATTACKS

No medicine or procedure will cure asthma. The key to asthma relief, therefore, is to prevent attacks and to relieve attack symptoms if they do occur.

A successful prevention plan* will do the following:

  1. Keep your activities, including exercise, at normal levels.
  2. Keep your lungs functioning normally or at a near-normal level.
  3. Prevent symptoms such as coughing or breathlessness that can keep you up at night, or occur in the early morning hours, or after exertion.
  4. Prevent asthma attacks from happening.
  5. Avoid unpleasant or harmful side effects that may result from using asthma medicine.

The best way to prevent asthma attacks is to avoid the triggers that bother you or your child. Try to identify the specific things that cause problems for you - things such as certain foods, house dust, or animal dander. Avoiding these triggers may be difficult or unpleasant. You may need to find a new home for a family pet or remove a carpet or a favorite stuffed toy. Even though these steps are difficult, they may be necessary in order to help prevent asthma attacks.

If house dust is a trigger, remove dust-collectors such as feather pillows, mattresses, quilts, and carpets from the bedroom. Mattresses and pillows can be covered with allergen-free covers. If a certain food triggers attacks, keep it out of your diet. Irritants in the air can be reduced by air conditioning, electrostatic air filters, or small-pore (HEPA) filters. Be careful of certain medicines. Aspirin and aspirin-like pain relievers, for example, can trigger attacks in some people and should be avoided if they do.

* Adapted from the National Heart, Lung, and Blood Institute: Guidelines for the Diagnosis and Management of Asthma. National Asthma Education Program, Expert Panel Report, 1991.

OTHER DO S AND DON TS

Anyone with asthma should stick to a healthy, balanced diet, get lots of rest and moderate exercise, and follow these do s and don ts:

cat graphic
  1. Don t smoke, and don t stay in the same room with people that do.
  2. Avoid fresh paint.
  3. Avoid sudden changes of temperature. Don t go in and out of extremely cool air-conditioned buildings during hot weather.
  4. Stay home in extremely cold weather, if possible.
  5. Stay away from people with cold or flu.
  6. Try to avoid emotionally upsetting situations.
  7. Drink lots of liquids.
  8. Don t overdo, but follow a regular exercise plan, including activities that help develop lung capacity.
  9. Don t take any medicine on your own without asking your doctor first.
  10. Take all medicines your doctor prescribes, as much and as often as you are told.
  11. Avoid taking sleeping pills or sedatives, even if asthma keeps you awake. Prop yourself up with extra pillows until your asthma medicine takes effect.
  12. Avoid breathing in insecticides, deodorants, cleaning fluids, chlorine, or other irritating gases.

ASTHMA MEDICINES

Preventive Medicine

no smoking graphic

Your doctor knows that, besides relieving an attack when it happens, it is also important to prevent attacks from occurring in the first place. Therefore, he or she has prescribed for you cromolyn sodium, a medicine that prevents asthma attacks by making airways less sensitive to asthma triggers. It works by stabilizing cells in the airway lining called mast cells. During an asthma attack, these cells become unstable and give off chemicals called mediators that cause inflammation and asthma attacks.

By preventing mediator release, cromolyn sodium works to prevent asthma attacks.

Bronchodilators

When someone is having an asthma attack, he or she needs a medicine called a bronchodilator to open up (dilate) the blocked airways in order to relieve asthma attacks. Your doctor may have already prescribed this medicine for you to use at that time.

HOW WILL CROMOLYN SODIUM WORK FOR YOU?

To get the best possible results, follow your doctor s instructions carefully when you first take cromolyn sodium.

Your doctor may tell you to take cromolyn sodium 10 to 15 minutes before you exercise or come into contact with a specific trigger, such as a cat. Usually, however, you will be told to take cromolyn sodium on a regular basis, probably starting at four times a day. It is crucial that you take cromolyn sodium, regularly, as often as your doctor recommends, even though you have no asthma symptoms at the time. Cromolyn sodium starts working right away but when you first begin taking it, you may have a lot of inflammation in your airways. Therefore, it may take up to two weeks (or perhaps one month) of regular treatment to bring your asthma under control. Do not stop taking cromolyn sodium or skip any doses without first talking with your doctor.

When you start using cromolyn sodium for the first time, your doctor may ask you to keep a diary showing when you have any symptoms, if and when you have trouble sleeping, how often you wheeze or cough, and other notes to help determine how effective cromolyn sodium will be to help you prevent asthma attacks. Your doctor may also recommend the use of a peak flow meter daily to help you better assess your progress.

While taking cromolyn sodium on a regular basis, you may need to take a bronchodilator-type medicine to treat occasional symptoms or attacks. While taking cromolyn sodium, you should continue taking your other medications until your doctor advises you otherwise.

HOW TO TAKE CROMOLYN SODIUM

Be sure to follow instructions carefully when you are shown how to take cromolyn sodium inhalation solution.

CARE AND STORAGE

Cromolyn sodium nebulizer solution should be stored at 20 to 25 C (68 to 77 F) [See USP Controlled Room Temperature].

Retain in foil pouch until time of use. PROTECT FROM LIGHT.

Do not use if it contains a precipitate (particles or cloudiness) or becomes discolored.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

NOTE: In case of difficulty consult your doctor or pharmacist

lungs graphic

Instructions for the Use of

CROMOLYN SODIUM INHALATION SOLUTION USP

An aqueous solution for nebulization

NOT FOR INJECTION

For best results, follow these instructions exactly and observe Care and Storage directions.

METHOD OF ADMINISTRATION

Cromolyn sodium inhalation solution is recommended for use in a power driven nebulizer operated at an airflow rate of 6 to 8 liters per minute and equipped with a suitable face mask. Hand-operated nebulizers are not suitable for the administration of cromolyn sodium inhalation solution. Your doctor will advise on the choice of a suitable nebulizer and how it should be used. Do not use any appliance without consulting your doctor.

Drug stability and safety of cromolyn sodium inhalation solution when mixed with other drugs in a nebulizer have not been established.

DOSAGE

Nebulization should be carried out four times a day at regular intervals, or as directed by your doctor. Use the contents of a fresh vial each time.

INHALATION

Once the nebulizer has been assembled and contains cromolyn sodium inhalation solution, hold the mask close to the patient s face and switch on the device. The patient should breathe in through the mouth and out through the nose in a normal, relaxed manner. Nebulization should take approximately five to ten minutes.

1. Remove a single unit-dose vial from strip (Figure 1).

Figure 1

Figure 1

2. Open the unit-dose vial by twisting off the tabbed top section (Figure 2).

Figure 2

Figure 2

3. Squeeze the contents of the unit-dose vial into the solution container of your nebulizer (Figure 3).

Figure 3

Figure 3

Discard the empty unit-dose vial.

Manufactured In England By:

Norton Healthcare Limited T/A IVAX Pharmaceuticals UK

Runcorn, Cheshire WA7 3FA England

Manufactured For:

TEVA PHARMACEUTICALS USA, INC.

North Wales, PA 19454

Rev. A 10/2015

Package/label Display Panel, Part 2 Of 2 

Cromolyn Sodium Inhalation Solution 20 mg/2 mL 60 Unit-Dose Vials Carton, Part 2 of 2

Cromolyn Sodium Inhalation Solution 20 mg/2 mL 60 Unit-Dose Vials Carton Text

NDC 0172-6406-49

Cromolyn Sodium
Inhalation Solution USP

20 mg/2 mL

Steri-Neb brand of Sterile Unit-Dose Vials
For Oral Inhalation Use Only
Not for Injection
Aqueous Solution for Nebulization
PRESERVATIVE FREE

Rx only

12 pouches of five 2 mL vials each (60 unit-dose vials)

TEVA

CROMOLYN SODIUM
cromolyn sodium solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0172-6406
Route of Administration INTRABRONCHIAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CROMOLYN SODIUM (UNII: Q2WXR1I0PK) (CROMOLYN - UNII:Y0TK0FS77W) CROMOLYN SODIUM 20 mg in 2 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0172-6406-49 60 in 1 CARTON 01/18/2000
1 NDC:0172-6406-05 2 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
2 NDC:0172-6406-59 120 in 1 CARTON 01/18/2000 09/30/2016
2 NDC:0172-6406-05 2 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075271 01/18/2000
Labeler - Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 2/2016 Teva Pharmaceuticals USA, Inc.

 

For Oral Inhalation Use Only - Not for Injection

Living A Full Life With Asthma  

PATIENT INSTRUCTIONS

CROMOLYN SODIUM INHALATION SOLUTION USP

You or your child may be among the millions of Americans who have asthma. For most patients, asthma need not limit your lifestyle, if you closely follow the asthma management plan your doctor provides you. Your doctor has given you this instruction sheet to help you learn more about asthma and ways to control it.

WHAT IS ASTHMA?

Asthma is a disease that causes patients to have difficulty breathing. Asthma attacks occur when the air passages (airways) to the lungs close up, blocking air from passing through. The closing up is caused by two things:

1.
The muscles around the airways tighten (constrict) making the airway narrower, and
2.
The passage lining swells and produces larger amounts of mucus (a sticky liquid normally found in airways). This swelling is caused by a certain type of inflammation that can build up in the airways of patients with asthma. Inflammation and the airway sensitivity that results from it cause further attacks to occur.
airway graphic

WHAT CAUSES THESE ATTACKS?

Asthma experts know that patients with asthma have attacks because their airways are inflamed and over reactive. Their lungs become super-sensitive to certain irritants or triggers , such as cold dry air, pollen, smoke, or cat dander. In the presence of such triggers, someone with asthma may have an attack, and attacks may occur more often.

Asthma triggers fall into 6 categories:

1.
Substances that cause allergies (pollens, animal dander, molds, house dust, some foods and medicines)
2.
Infections that affect breathing (colds, flu)
3.
Emotional stress (difficult situations at home, school, or work)
4.
Strenuous exercise
5.
Irritating gases (chlorine, perfume, tobacco smoke)
6.
Sudden changes in temperature or humidity
pollen graphic

HOW TO PREVENT ASTHMA ATTACKS

No medicine or procedure will cure asthma. The key to asthma relief, therefore, is to prevent attacks and to relieve attack symptoms if they do occur.

A successful prevention plan* will do the following:

1.
Keep your activities, including exercise, at normal levels.
2.
Keep your lungs functioning normally or at a near-normal level.
3.
Prevent symptoms such as coughing or breathlessness that can keep you up at night, or occur in the early morning hours, or after exertion.
4.
Prevent asthma attacks from happening.
5.
Avoid unpleasant or harmful side effects that may result from using asthma medicine.

The best way to prevent asthma attacks is to avoid the triggers that bother you or your child. Try to identify the specific things that cause problems for you - things such as certain foods, house dust, or animal dander. Avoiding these triggers may be difficult or unpleasant. You may need to find a new home for a family pet or remove a carpet or a favorite stuffed toy. Even though these steps are difficult, they may be necessary in order to help prevent asthma attacks.

If house dust is a trigger, remove dust-collectors such as feather pillows, mattresses, quilts, and carpets from the bedroom. Mattresses and pillows can be covered with allergen-free covers. If a certain food triggers attacks, keep it out of your diet. Irritants in the air can be reduced by air conditioning, electrostatic air filters, or small-pore (HEPA) filters. Be careful of certain medicines. Aspirin and aspirin-like pain relievers, for example, can trigger attacks in some people and should be avoided if they do.

* Adapted from the National Heart, Lung, and Blood Institute: Guidelines for the Diagnosis and Management of Asthma. National Asthma Education Program, Expert Panel Report, 1991.

OTHER DO S AND DON TS

Anyone with asthma should stick to a healthy, balanced diet, get lots of rest and moderate exercise, and follow these do s and don ts:

cat graphic
1.
Don t smoke, and don t stay in the same room with people that do.
2.
Avoid fresh paint.
3.
Avoid sudden changes of temperature. Don t go in and out of extremely cool air-conditioned buildings during hot weather.
4.
Stay home in extremely cold weather, if possible.
5.
Stay away from people with cold or flu.
6.
Try to avoid emotionally upsetting situations.
7.
Drink lots of liquids.
8.
Don t overdo, but follow a regular exercise plan, including activities that help develop lung capacity.
9.
Don t take any medicine on your own without asking your doctor first.
10.
Take all medicines your doctor prescribes, as much and as often as you are told.
11.
Avoid taking sleeping pills or sedatives, even if asthma keeps you awake. Prop yourself up with extra pillows until your asthma medicine takes effect.
12.
Avoid breathing in insecticides, deodorants, cleaning fluids, chlorine, or other irritating gases.

ASTHMA MEDICINES

Preventive Medicine

no smoking graphic

Your doctor knows that, besides relieving an attack when it happens, it is also important to prevent attacks from occurring in the first place. Therefore, he or she has prescribed for you cromolyn sodium, a medicine that prevents asthma attacks by making airways less sensitive to asthma triggers. It works by stabilizing cells in the airway lining called mast cells. During an asthma attack, these cells become unstable and give off chemicals called mediators that cause inflammation and asthma attacks.

By preventing mediator release, cromolyn sodium works to prevent asthma attacks.

Bronchodilators

When someone is having an asthma attack, he or she needs a medicine called a bronchodilator to open up (dilate) the blocked airways in order to relieve asthma attacks. Your doctor may have already prescribed this medicine for you to use at that time.

HOW WILL CROMOLYN SODIUM WORK FOR YOU?

To get the best possible results, follow your doctor s instructions carefully when you first take cromolyn sodium.

Your doctor may tell you to take cromolyn sodium 10 to 15 minutes before you exercise or come into contact with a specific trigger, such as a cat. Usually, however, you will be told to take cromolyn sodium on a regular basis, probably starting at four times a day. It is crucial that you take cromolyn sodium, regularly, as often as your doctor recommends, even though you have no asthma symptoms at the time. Cromolyn sodium starts working right away but when you first begin taking it, you may have a lot of inflammation in your airways. Therefore, it may take up to two weeks (or perhaps one month) of regular treatment to bring your asthma under control. Do not stop taking cromolyn sodium or skip any doses without first talking with your doctor.

When you start using cromolyn sodium for the first time, your doctor may ask you to keep a diary showing when you have any symptoms, if and when you have trouble sleeping, how often you wheeze or cough, and other notes to help determine how effective cromolyn sodium will be to help you prevent asthma attacks. Your doctor may also recommend the use of a peak flow meter daily to help you better assess your progress.

While taking cromolyn sodium on a regular basis, you may need to take a bronchodilator-type medicine to treat occasional symptoms or attacks. While taking cromolyn sodium, you should continue taking your other medications until your doctor advises you otherwise.

HOW TO TAKE CROMOLYN SODIUM

Be sure to follow instructions carefully when you are shown how to take cromolyn sodium inhalation solution.

CARE AND STORAGE

Cromolyn sodium nebulizer solution should be stored at 20 to 25 C (68 to 77 F) [See USP Controlled Room Temperature].

Retain in foil pouch until time of use. PROTECT FROM LIGHT.

Do not use if it contains a precipitate (particles or cloudiness) or becomes discolored.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

NOTE: In case of difficulty consult your doctor or pharmacist

lungs graphic

Instructions for the Use of

CROMOLYN SODIUM INHALATION SOLUTION USP

An aqueous solution for nebulization

NOT FOR INJECTION

For best results, follow these instructions exactly and observe Care and Storage directions.

METHOD OF ADMINISTRATION

Cromolyn sodium inhalation solution is recommended for use in a power driven nebulizer operated at an airflow rate of 6 to 8 liters per minute and equipped with a suitable face mask. Hand-operated nebulizers are not suitable for the administration of cromolyn sodium inhalation solution. Your doctor will advise on the choice of a suitable nebulizer and how it should be used. Do not use any appliance without consulting your doctor.

Drug stability and safety of cromolyn sodium inhalation solution when mixed with other drugs in a nebulizer have not been established.

DOSAGE

Nebulization should be carried out four times a day at regular intervals, or as directed by your doctor. Use the contents of a fresh vial each time.

INHALATION

Once the nebulizer has been assembled and contains cromolyn sodium inhalation solution, hold the mask close to the patient s face and switch on the device. The patient should breathe in through the mouth and out through the nose in a normal, relaxed manner. Nebulization should take approximately five to ten minutes.

1. Remove a single unit-dose vial from strip (Figure 1).

Figure 1

Figure 1

2. Open the unit-dose vial by twisting off the tabbed top section (Figure 2).

Figure 2

Figure 2

3. Squeeze the contents of the unit-dose vial into the solution container of your nebulizer (Figure 3).

Figure 3

Figure 3

Discard the empty unit-dose vial.

Manufactured for:
Ailex Pharmaceuticals, LLC
Lenexa, KS 66215

Rev.: 06/2016



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