"68788-8182-2" National Drug Code (NDC)

Ibuprofen 20 TABLET, FILM COATED in 1 BOTTLE (68788-8182-2)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8182-2
Package Description20 TABLET, FILM COATED in 1 BOTTLE (68788-8182-2)
Product NDC68788-8182
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220428
Marketing Category NameANDA
Application NumberANDA202413
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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