"70518-0715-0" National Drug Code (NDC)

NDC Code	70518-0715-0
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0715-0)
Product NDC	70518-0715
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Abacavir And Lamivudine
Non-Proprietary Name	Abacavir And Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20170828
Marketing Category Name	ANDA
Application Number	ANDA204990
Manufacturer	REMEDYREPACK INC.
Substance Name	ABACAVIR SULFATE; LAMIVUDINE
Strength	600; 300
Strength Unit	mg/1; mg/1
Pharmacy Classes	Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]