"50436-0319-7" National Drug Code (NDC)

Ibuprofen 12 TABLET, FILM COATED in 1 BOTTLE (50436-0319-7)
(Unit Dose Services)

NDC Code50436-0319-7
Package Description12 TABLET, FILM COATED in 1 BOTTLE (50436-0319-7)
Product NDC50436-0319
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151221
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerUnit Dose Services
Substance NameIBUPROFEN
Strength400
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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