"57237-062-90" National Drug Code (NDC)

NDC Code	57237-062-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (57237-062-90)
Product NDC	57237-062
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Finasteride
Non-Proprietary Name	Finasteride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20071030
Marketing Category Name	ANDA
Application Number	ANDA078341
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	FINASTERIDE
Strength	5
Strength Unit	mg/1
Pharmacy Classes	5-alpha Reductase Inhibitor [EPC], 5-alpha Reductase Inhibitors [MoA]