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"70518-0559-0" National Drug Code (NDC)

Abacavir 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0559-0)
(REMEDYREPACK INC.)

NDC Code70518-0559-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0559-0)
Product NDC70518-0559
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAbacavir
Non-Proprietary NameAbacavir
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170530
Marketing Category NameANDA
Application NumberANDA077844
ManufacturerREMEDYREPACK INC.
Substance NameABACAVIR SULFATE
Strength300
Strength Unitmg/1
Pharmacy ClassesHuman 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/70518-0559-0





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