"0074-0039-01" National Drug Code (NDC)

NDC Code	0074-0039-01
Package Description	1 BLISTER PACK in 1 CARTON (0074-0039-01) > 14 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	0074-0039
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Orilissa
Non-Proprietary Name	Elagolix
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180723
Marketing Category Name	NDA
Application Number	NDA210450
Manufacturer	AbbVie Inc.
Substance Name	ELAGOLIX SODIUM
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Decreased GnRH Secretion [PE], Gonadotropin Releasing Hormone Receptor Antagonist [EPC], Gonadotropin Releasing Hormone Receptor Antagonists [MoA], P-Glycoprotein Inhibitors [MoA]