"75987-010-03" National Drug Code (NDC)

Duexis 90 TABLET, COATED in 1 BOTTLE (75987-010-03)
(Horizon Therapeutics USA, Inc.)

NDC Code75987-010-03
Package Description90 TABLET, COATED in 1 BOTTLE (75987-010-03)
Product NDC75987-010
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDuexis
Non-Proprietary NameIbuprofen And Famotidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20111205
End Marketing Date20250831
Marketing Category NameNDA
Application NumberNDA022519
ManufacturerHorizon Therapeutics USA, 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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