"68788-7298-4" National Drug Code (NDC)

NDC Code	68788-7298-4
Package Description	6 TABLET, FILM COATED in 1 BOTTLE (68788-7298-4)
Product NDC	68788-7298
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	20190104
Marketing Category Name	ANDA
Application Number	ANDA079124
Manufacturer	Preferred Pharmaceuticals Inc.
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]