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"68788-8897-9" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8897-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68788-8897-9)
Product NDC68788-8897
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250801
Marketing Category NameANDA
Application NumberANDA211890
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameFAMOTIDINE; IBUPROFEN
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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