"50268-456-12" National Drug Code (NDC)

NDC Code	50268-456-12
Package Description	20 BLISTER PACK in 1 BOX (50268-456-12) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-456-11)
Product NDC	50268-456
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	20200512
Marketing Category Name	ANDA
Application Number	ANDA079124
Manufacturer	AvPAK
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], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA]