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"75987-010-71" National Drug Code (NDC)

Duexis 15 BLISTER PACK in 1 BLISTER PACK (75987-010-71) > 1 TABLET, COATED in 1 BLISTER PACK
(Horizon Pharma Inc.)

NDC Code75987-010-71
Package Description15 BLISTER PACK in 1 BLISTER PACK (75987-010-71) > 1 TABLET, COATED in 1 BLISTER PACK
Product NDC75987-010
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuexis
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20110429
Marketing Category NameNDA
Application NumberNDA022519
ManufacturerHorizon Pharma Inc.
Substance NameFAMOTIDINE; IBUPROFEN
Strength26.6; 800
Strength Unitmg/1; mg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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