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Finasteride - 55111-171-05 - (Finasteride)

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Drug Information of Finasteride

Product NDC: 55111-171
Proprietary Name: Finasteride
Non Proprietary Name: Finasteride
Active Ingredient(s): 1    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: 55111-171
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076436
Marketing Category: ANDA
Start Marketing Date: 20130102

Package Information of Finasteride

Package NDC: 55111-171-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)

NDC Information of Finasteride

NDC Code 55111-171-05
Proprietary Name Finasteride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)
Product NDC 55111-171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130102
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name FINASTERIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

Complete Information of Finasteride


General Information