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Finasteride - 65977-5025-3 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 65977-5025
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: 65977-5025
Labeler Name: Hetero Drugs Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090061
Marketing Category: ANDA
Start Marketing Date: 20100607

Package Information of Finasteride

Package NDC: 65977-5025-3
Package Description: 48 BOTTLE in 1 CONTAINER (65977-5025-3) > 90 TABLET in 1 BOTTLE

NDC Information of Finasteride

NDC Code 65977-5025-3
Proprietary Name Finasteride
Package Description 48 BOTTLE in 1 CONTAINER (65977-5025-3) > 90 TABLET in 1 BOTTLE
Product NDC 65977-5025
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100607
Marketing Category Name ANDA
Labeler Name Hetero Drugs Limited
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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