"63717-900-99" National Drug Code (NDC)

Reprexain 1 TABLET, FILM COATED in 1 PACKET (63717-900-99)
(Hawthorn Pharmaceuticals, Inc.)

NDC Code63717-900-99
Package Description1 TABLET, FILM COATED in 1 PACKET (63717-900-99)
Product NDC63717-900
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameReprexain
Non-Proprietary NameHydrocodone Bitartrate, Ibuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20081216
Marketing Category NameANDA
Application NumberANDA076642
ManufacturerHawthorn Pharmaceuticals, Inc.
Substance NameHYDROCODONE BITARTRATE; IBUPROFEN
Strength2.5; 200
Strength Unitmg/1; mg/1
Pharmacy ClassesOpioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
DEA ScheduleCIII

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