"67979-002-01" National Drug Code (NDC)

NDC Code	67979-002-01
Package Description	1 VIAL, GLASS in 1 CARTON (67979-002-01) / 1 IMPLANT in 1 VIAL, GLASS
Product NDC	67979-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Supprelin
Proprietary Name Suffix	La
Non-Proprietary Name	Histrelin Acetate
Dosage Form	IMPLANT
Usage	SUBCUTANEOUS
Start Marketing Date	20070531
Marketing Category Name	NDA
Application Number	NDA022058
Manufacturer	ENDO USA, Inc.
Substance Name	HISTRELIN ACETATE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Gonadotropin Releasing Hormone Receptor Agonist [EPC], Gonadotropin Releasing Hormone Receptor Agonists [MoA]