"70518-0640-0" National Drug Code (NDC)

Abacavir Sulfate 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0640-0)
(REMEDYREPACK INC.)

NDC Code70518-0640-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0640-0)
Product NDC70518-0640
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAbacavir Sulfate
Non-Proprietary NameAbacavir Sulfate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170726
Marketing Category NameANDA
Application NumberANDA201570
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]

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