"70518-2067-0" National Drug Code (NDC)

Lamivudine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2067-0)
(REMEDYREPACK INC.)

NDC Code70518-2067-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2067-0)
Product NDC70518-2067
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190508
Marketing Category NameANDA
Application NumberANDA090457
ManufacturerREMEDYREPACK 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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