"69396-172-01" National Drug Code (NDC)

Ibuprofen 1000 TABLET in 1 BOTTLE (69396-172-01)
(Trifecta Pharmaceuticals USA LLC)

NDC Code69396-172-01
Package Description1000 TABLET in 1 BOTTLE (69396-172-01)
Product NDC69396-172
Product Type NameHUMAN OTC DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20230808
Marketing Category NameANDA
Application NumberANDA207095
ManufacturerTrifecta Pharmaceuticals USA LLC
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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