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ALDACTONE- spironolactone tablet, film coated


  1. Patient Information
  2. Active Ingredient(s):
  3. Inactive Ingredient(s):
  4. Revised: 9/2019document Id:

Patient Information 

Patients who receive ALDACTONE should be advised to avoid potassium supplements and foods containing high levels of potassium, including salt substitutes.

This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com.

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LAB-0231-13.0

DRUG: Aldactone

GENERIC: spironolactone

DOSAGE: TABLET, FILM COATED

ADMINSTRATION: ORAL

NDC: 70518-1396-0

COLOR: yellow

SHAPE: ROUND

SCORE: No score

SIZE: 9 mm

IMPRINT: SEARLE;1001;ALDACTONE;25

PACKAGING: 30 in 1 BLISTER PACK

Active Ingredient(s): 

  • SPIRONOLACTONE 25mg in 1

Inactive Ingredient(s): 

  • CALCIUM SULFATE DIHYDRATE
  • PEPPERMINT
  • HYPROMELLOSE 2910 (15000 MPA.S)
  • CARNAUBA WAX
  • POLYETHYLENE GLYCOL 400
  • STARCH, CORN
  • FERRIC OXIDE RED
  • MAGNESIUM STEARATE
  • STEARIC ACID
  • POVIDONE, UNSPECIFIED
  • TITANIUM DIOXIDE

Remedy_Label

ALDACTONE
spironolactone tablet, film coated
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70518-1396(NDC:0025-1001)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SPIRONOLACTONE(UNII: 27O7W4T232) (SPIRONOLACTONE - UNII:27O7W4T232)SPIRONOLACTONE25 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN(UNII: O8232NY3SJ)
FERRIC OXIDE RED(UNII: 1K09F3G675)
MAGNESIUM STEARATE(UNII: 70097M6I30)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
HYPROMELLOSE 2910 (15000 MPA.S)(UNII: 288VBX44JC)
CALCIUM SULFATE DIHYDRATE(UNII: 4846Q921YM)
PEPPERMINT(UNII: V95R5KMY2B)
POLYETHYLENE GLYCOL 400(UNII: B697894SGQ)
CARNAUBA WAX(UNII: R12CBM0EIZ)
STEARIC ACID(UNII: 4ELV7Z65AP)
Product Characteristics
Coloryellow (light yellow)Scoreno score
ShapeROUNDSize9mm
FlavorImprint CodeSEARLE;1001;ALDACTONE;25
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70518-1396-030 in 1 BLISTER PACK; Type 0: Not a Combination Product08/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01215108/31/2018
Labeler -REMEDYREPACK INC. (829572556)

Revised: 9/2019document Id: 

92bb1ecf-acd9-c81d-e053-2995a90a593cSet id: db1e617e-3245-46bb-a8c2-776451db7e19Version: 3Effective Time: 20190917REMEDYREPACK INC.



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