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Finasteride - 54868-5636-2 - (finasteride)

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Drug Information of Finasteride

Product NDC: 54868-5636
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: 54868-5636
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077914
Marketing Category: ANDA
Start Marketing Date: 20060630

Package Information of Finasteride

Package NDC: 54868-5636-2
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5636-2)

NDC Information of Finasteride

NDC Code 54868-5636-2
Proprietary Name Finasteride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5636-2)
Product NDC 54868-5636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060630
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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