"68084-578-21" National Drug Code (NDC)

NDC Code	68084-578-21
Package Description	30 BLISTER PACK in 1 CARTON (68084-578-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-578-11)
Product NDC	68084-578
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120217
End Marketing Date	20181130
Marketing Category Name	ANDA
Application Number	ANDA202032
Manufacturer	American Health Packaging
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]