"49349-905-02" National Drug Code (NDC)

Ziagen 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-905-02)
(REMEDYREPACK INC.)

NDC Code49349-905-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-905-02)
Product NDC49349-905
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZiagen
Non-Proprietary NameAbacavir Sulfate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130408
Marketing Category NameNDA
Application NumberNDA020977
ManufacturerREMEDYREPACK INC.
Substance NameABACAVIR SULFATE
Strength300
Strength Unitmg/1
Pharmacy ClassesHuman Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

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