"53808-0990-1" National Drug Code (NDC)

NDC Code	53808-0990-1
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0990-1)
Product NDC	53808-0990
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Trizivir
Non-Proprietary Name	Abacavir Sulfate, Lamivudine, And Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20130201
Marketing Category Name	NDA
Application Number	NDA021205
Manufacturer	State of Florida DOH Central Pharmacy
Substance Name	ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE
Strength	300; 150; 300
Strength Unit	mg/1; 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],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]