"55801-314-01" National Drug Code (NDC)

NDC Code	55801-314-01
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (55801-314-01)
Product NDC	55801-314
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170201
Marketing Category Name	ANDA
Application Number	ANDA206974
Manufacturer	APPCO PHARMA LLC
Substance Name	LAMIVUDINE
Strength	300
Strength Unit	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]