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"70518-1634-0" National Drug Code (NDC)

Lamivudine 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1634-0)
(REMEDYREPACK INC.)

NDC Code70518-1634-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1634-0)
Product NDC70518-1634
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181105
Marketing Category NameANDA
Application NumberANDA203277
ManufacturerREMEDYREPACK INC.
Substance NameLAMIVUDINE
Strength300
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1634-0





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