"76519-1204-3" National Drug Code (NDC)

NDC Code	76519-1204-3
Package Description	30 TABLET, FILM COATED in 1 VIAL, PLASTIC (76519-1204-3)
Product NDC	76519-1204
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Finasteride
Non-Proprietary Name	Finasteride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180426
Marketing Category Name	ANDA
Application Number	ANDA091643
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	FINASTERIDE
Strength	1
Strength Unit	mg/1
Pharmacy Classes	5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]