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Finasteride - 43598-303-90 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 43598-303
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: 43598-303
Labeler Name: Dr Reddys Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090061
Marketing Category: ANDA
Start Marketing Date: 20121025

Package Information of Finasteride

Package NDC: 43598-303-90
Package Description: 90 TABLET in 1 BOTTLE (43598-303-90)

NDC Information of Finasteride

NDC Code 43598-303-90
Proprietary Name Finasteride
Package Description 90 TABLET in 1 BOTTLE (43598-303-90)
Product NDC 43598-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121025
Marketing Category Name ANDA
Labeler Name Dr Reddys Laboratories 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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