"72865-172-30" National Drug Code (NDC)

NDC Code	72865-172-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (72865-172-30)
Product NDC	72865-172
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Efavirenz
Non-Proprietary Name	Efavirenz
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20210529
Marketing Category Name	ANDA
Application Number	ANDA078886
Manufacturer	XLCare Pharmaceuticals Inc.
Substance Name	EFAVIRENZ
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]