"66993-482-30" National Drug Code (NDC)

NDC Code	66993-482-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (66993-482-30)
Product NDC	66993-482
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Abacavir And Lamivudine
Non-Proprietary Name	Abacavir Sulfate And Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20160929
End Marketing Date	20201231
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA021652
Manufacturer	Prasco Laboratories
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]