"49349-885-04" National Drug Code (NDC)

NDC Code	49349-885-04
Package Description	14 TABLET, FILM COATED in 1 BLISTER PACK (49349-885-04)
Product NDC	49349-885
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20130411
Marketing Category Name	ANDA
Application Number	ANDA202032
Manufacturer	REMEDYREPACK INC.
Substance Name	LAMIVUDINE
Strength	150
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]