"0093-5382-56" National Drug Code (NDC)

NDC Code	0093-5382-56
Package Description	1 BOTTLE in 1 CARTON (0093-5382-56) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC	0093-5382
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	20160929
End Marketing Date	20211130
Marketing Category Name	ANDA
Application Number	ANDA079246
Manufacturer	Teva Pharmaceuticals USA, Inc.
Substance Name	ABACAVIR SULFATE; LAMIVUDINE
Strength	600; 300
Strength Unit	mg/1; mg/1
Pharmacy Classes	Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]