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"72189-667-90" National Drug Code (NDC)

Ibuprofen Famotidine 90 TABLET in 1 BOTTLE (72189-667-90)
(Direct_Rx)

NDC Code72189-667-90
Package Description90 TABLET in 1 BOTTLE (72189-667-90)
Product NDC72189-667
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen Famotidine
Non-Proprietary NameIbuprofen Famotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20260622
Marketing Category NameANDA
Application NumberANDA218684
ManufacturerDirect_Rx
Substance NameIBUPROFEN; FAMOTIDINE
Strength26.6; 800
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

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