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Finasteride - 52125-606-02 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 52125-606
Proprietary Name: Finasteride
Non Proprietary Name: Finasteride
Active Ingredient(s): 5    mg/1 & nbsp;   Finasteride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Finasteride

Product NDC: 52125-606
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090061
Marketing Category: ANDA
Start Marketing Date: 20130529

Package Information of Finasteride

Package NDC: 52125-606-02
Package Description: 30 TABLET in 1 VIAL (52125-606-02)

NDC Information of Finasteride

NDC Code 52125-606-02
Proprietary Name Finasteride
Package Description 30 TABLET in 1 VIAL (52125-606-02)
Product NDC 52125-606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130529
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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