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Finasteride - 63739-495-41 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 63739-495
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: 63739-495
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077914
Marketing Category: ANDA
Start Marketing Date: 20101122

Package Information of Finasteride

Package NDC: 63739-495-41
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63739-495-41)

NDC Information of Finasteride

NDC Code 63739-495-41
Proprietary Name Finasteride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63739-495-41)
Product NDC 63739-495
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101122
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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


General Information