"31722-001-02" National Drug Code (NDC)

NDC Code	31722-001-02
Package Description	20 BLISTER PACK in 1 CARTON (31722-001-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	31722-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine
Non-Proprietary Name	Lamivudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20190321
Marketing Category Name	ANDA
Application Number	ANDA211306
Manufacturer	Camber Pharmaceuticals, Inc.
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 [EXT], Nucleoside Reverse Transcriptase Inhibitors [MoA]