"61919-061-02" National Drug Code (NDC)

NDC Code	61919-061-02
Package Description	2 TABLET in 1 BOTTLE (61919-061-02)
Product NDC	61919-061
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine Zidovudine
Non-Proprietary Name	Lamivudine Zidovudine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150101
Marketing Category Name	ANDA
Application Number	ANDA202418
Manufacturer	Direct Rx
Substance Name	LAMIVUDINE; ZIDOVUDINE
Strength	150; 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 Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]