"72974-120-97" National Drug Code (NDC)

NDC Code	72974-120-97
Package Description	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72974-120-97)
Product NDC	72974-120
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Orgovyx
Non-Proprietary Name	Relugolix
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20201218
Marketing Category Name	NDA
Application Number	NDA214621
Manufacturer	Sumitomo Pharma America, Inc
Substance Name	RELUGOLIX
Strength	120
Strength Unit	mg/1
Pharmacy Classes	Breast Cancer Resistance Protein Inhibitors [MoA], Cytochrome P450 2B6 Inducers [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]