Home > National Drug Code (NDC) > Finasteride

Finasteride - 0378-3151-77 - (finasteride)

Alphabetical Index


Drug Information of Finasteride

Product NDC: 0378-3151
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: 0378-3151
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077578
Marketing Category: ANDA
Start Marketing Date: 20110223

Package Information of Finasteride

Package NDC: 0378-3151-77
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3151-77)

NDC Information of Finasteride

NDC Code 0378-3151-77
Proprietary Name Finasteride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3151-77)
Product NDC 0378-3151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110223
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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


General Information