"60505-3251-0" National Drug Code (NDC)

NDC Code	60505-3251-0
Package Description	10 BLISTER PACK in 1 CARTON (60505-3251-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	60505-3251
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20111202
Marketing Category Name	ANDA
Application Number	ANDA091606
Manufacturer	Apotex Corp.
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]