"70786-0321-1" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BOTTLE (70786-0321-1)
(Unit Dose Services)

NDC Code70786-0321-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (70786-0321-1)
Product NDC70786-0321
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
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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