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"70748-312-09" National Drug Code (NDC)

Ibuprofen And Famotidine 90 TABLET, COATED in 1 BOTTLE (70748-312-09)
(Lupin Pharmaceuticals, Inc.)

NDC Code70748-312-09
Package Description90 TABLET, COATED in 1 BOTTLE (70748-312-09)
Product NDC70748-312
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen And Famotidine
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20210914
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022519
ManufacturerLupin 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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