"49349-713-12" National Drug Code (NDC)

NDC Code	49349-713-12
Package Description	8 TABLET in 1 BLISTER PACK (49349-713-12)
Product NDC	49349-713
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Epivir
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110420
End Marketing Date	20171116
Marketing Category Name	NDA
Application Number	NDA020564
Manufacturer	REMEDYREPACK INC.
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]