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Finasteride - 31722-526-10 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 31722-526
Proprietary Name: Finasteride
Non Proprietary Name: Finasteride
Active Ingredient(s): 1    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: 31722-526
Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090060
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Finasteride

Package NDC: 31722-526-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)

NDC Information of Finasteride

NDC Code 31722-526-10
Proprietary Name Finasteride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)
Product NDC 31722-526
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals, Inc.
Substance Name FINASTERIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

Complete Information of Finasteride


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