"31722-753-06" National Drug Code (NDC)

Lamivudine 600 TABLET, FILM COATED in 1 BOTTLE (31722-753-06)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-753-06
Package Description600 TABLET, FILM COATED in 1 BOTTLE (31722-753-06)
Product NDC31722-753
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140106
Marketing Category NameANDA
Application NumberANDA203277
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameLAMIVUDINE
Strength150
Strength Unitmg/1
Pharmacy ClassesHepatitis 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]

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