"70518-0176-1" National Drug Code (NDC)

Ibuprofen 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0176-1)
(REMEDYREPACK INC.)

NDC Code70518-0176-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0176-1)
Product NDC70518-0176
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170125
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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