Finasteride (Page 6 of 6)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Container Label for Finasteride Tablets, 1 mg 30s count

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Container Label for Finasteride Tablets, 1 mg 30s count

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Container Label for Finasteride Tablets, 1 mg 90s count

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Container Label for Finasteride Tablets, 1 mg 90s count

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Container Label for Finasteride Tablets, 1 mg 1000s count

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Container Label for Finasteride Tablets, 1 mg 1000s count

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FINASTERIDE finasteride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:31722-526
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FINASTERIDE (FINASTERIDE) FINASTERIDE 1 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE
CELLULOSE, MICROCRYSTALLINE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
DOCUSATE SODIUM
MAGNESIUM STEARATE
HYPROMELLOSES
FERRIC OXIDE RED
TALC
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
Product Characteristics
Color BROWN Score no score
Shape ROUND Size 7mm
Flavor Imprint Code H;36
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:31722-526-30 30 TABLET, FILM COATED in 1 BOTTLE None
2 NDC:31722-526-90 90 TABLET, FILM COATED in 1 BOTTLE None
3 NDC:31722-526-10 1000 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090060 07/01/2013
Labeler — Camber Pharmaceuticals, Inc. (826774775)

Revised: 07/2017 Camber Pharmaceuticals, Inc.

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