"70518-2284-0" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2284-0)
(REMEDYREPACK INC.)

NDC Code70518-2284-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2284-0)
Product NDC70518-2284
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190826
Marketing Category NameANDA
Application NumberANDA072096
ManufacturerREMEDYREPACK INC.
Substance NameIBUPROFEN
Strength200
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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