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Finasteride - 0093-7355-05 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 0093-7355
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: 0093-7355
Labeler Name: Teva Pharmaceuticals USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076511
Marketing Category: ANDA
Start Marketing Date: 20061215

Package Information of Finasteride

Package NDC: 0093-7355-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)

NDC Information of Finasteride

NDC Code 0093-7355-05
Proprietary Name Finasteride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)
Product NDC 0093-7355
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061215
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA
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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