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"70518-4580-0" National Drug Code (NDC)

Ibuprofen And Famotidine 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4580-0)
(REMEDYREPACK INC.)

NDC Code70518-4580-0
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4580-0)
Product NDC70518-4580
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260305
Marketing Category NameANDA
Application NumberANDA211890
ManufacturerREMEDYREPACK 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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