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Finasteride - 55111-172-01 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 55111-172
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: 55111-172
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076437
Marketing Category: ANDA
Start Marketing Date: 20070228

Package Information of Finasteride

Package NDC: 55111-172-01
Package Description: 100 TABLET in 1 BOTTLE (55111-172-01)

NDC Information of Finasteride

NDC Code 55111-172-01
Proprietary Name Finasteride
Package Description 100 TABLET in 1 BOTTLE (55111-172-01)
Product NDC 55111-172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070228
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories 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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