"50090-1419-0" National Drug Code (NDC)

NDC Code	50090-1419-0
Package Description	2 TABLET, FILM COATED in 1 BOTTLE (50090-1419-0)
Product NDC	50090-1419
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine And Zidovudine
Non-Proprietary Name	Lamivudine And Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120515
Marketing Category Name	ANDA
Application Number	ANDA202418
Manufacturer	A-S Medication Solutions
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 [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]