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Finasteride - 51079-520-56 - (finasteride)

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Drug Information of Finasteride

Product NDC: 51079-520
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: 51079-520
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077578
Marketing Category: ANDA
Start Marketing Date: 20120820

Package Information of Finasteride

Package NDC: 51079-520-56
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-520-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-520-30)

NDC Information of Finasteride

NDC Code 51079-520-56
Proprietary Name Finasteride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-520-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-520-30)
Product NDC 51079-520
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120820
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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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