PROPECIA - 54868-4120-0 - (finasteride)

Alphabetical Index


Drug Information of PROPECIA

Product NDC: 54868-4120
Proprietary Name: PROPECIA
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 PROPECIA

Product NDC: 54868-4120
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020788
Marketing Category: NDA
Start Marketing Date: 19971219

Package Information of PROPECIA

Package NDC: 54868-4120-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-4120-0)

NDC Information of PROPECIA

NDC Code 54868-4120-0
Proprietary Name PROPECIA
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-4120-0)
Product NDC 54868-4120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name finasteride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19971219
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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 PROPECIA


General Information