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FINASTERIDE - 47335-715-81 - (FINASTERIDE)

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Drug Information of FINASTERIDE

Product NDC: 47335-715
Proprietary Name: FINASTERIDE
Non Proprietary Name: FINASTERIDE
Active Ingredient(s): 5    mg/1 & nbsp;   FINASTERIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of FINASTERIDE

Product NDC: 47335-715
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090507
Marketing Category: ANDA
Start Marketing Date: 20110818

Package Information of FINASTERIDE

Package NDC: 47335-715-81
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)

NDC Information of FINASTERIDE

NDC Code 47335-715-81
Proprietary Name FINASTERIDE
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)
Product NDC 47335-715
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FINASTERIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110818
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name FINASTERIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

Complete Information of FINASTERIDE


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