"0179-0152-70" National Drug Code (NDC)

NDC Code	0179-0152-70
Package Description	30 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0179-0152-70)
Product NDC	0179-0152
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20140529
Marketing Category Name	ANDA
Application Number	ANDA202941
Manufacturer	KAISER FOUNDATION HOSPITALS
Substance Name	LAMIVUDINE
Strength	100
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]