"52125-016-02" National Drug Code (NDC)

Lamivudine 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-016-02)
(REMEDYREPACK INC.)

NDC Code52125-016-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-016-02)
Product NDC52125-016
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine
Non-Proprietary NameLamivudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130328
Marketing Category NameANDA
Application NumberANDA202032
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 [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

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