"65862-335-30" National Drug Code (NDC)

NDC Code	65862-335-30
Package Description	1 BOTTLE in 1 CARTON (65862-335-30) / 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC	65862-335
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	20181115
Marketing Category Name	ANDA
Application Number	ANDA090159
Manufacturer	Aurobindo Pharma Limited
Substance Name	ABACAVIR SULFATE; LAMIVUDINE
Strength	600; 300
Strength Unit	mg/1; mg/1
Pharmacy Classes	Cytochrome P450 1A1 Inhibitors [MoA], Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA]