Spironolactone (Page 5 of 5)

HOW SUPPLIED

NDC:68151-2776-1 in a BOTTLE of 1 TABLET, FILM COATEDS

SPIRONOLACTONE TABLET, FILM COATED

Label Image
(click image for full-size original)
SPIRONOLACTONE
spironolactone tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-2776(NDC:0228-2803)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SPIRONOLACTONE (SPIRONOLACTONE) SPIRONOLACTONE 25 mg
Inactive Ingredients
Ingredient Name Strength
CALCIUM SULFATE
STARCH, CORN
CROSPOVIDONE
DEXTROSE
HYPROMELLOSES
MAGNESIUM STEARATE
MALTODEXTRIN
PEPPERMINT
POLYETHYLENE GLYCOLS
POVIDONE K29/32
POLYDEXTROSE
SILICON DIOXIDE
TITANIUM DIOXIDE
TRIACETIN
Product Characteristics
Color WHITE (to off-white) Score no score
Shape ROUND Size 7mm
Flavor Imprint Code R;803
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-2776-1 1 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040353 01/03/2007
Labeler — Carilion Materials Management (079239644)
Registrant — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-2776)

Revised: 03/2015 Carilion Materials Management

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