"70518-1013-0" National Drug Code (NDC)

NDC Code	70518-1013-0
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1013-0)
Product NDC	70518-1013
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Efavirenz
Non-Proprietary Name	Efavirenz
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180212
Marketing Category Name	ANDA
Application Number	ANDA091471
Manufacturer	REMEDYREPACK INC.
Substance Name	EFAVIRENZ
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA]