"63717-902-01" National Drug Code (NDC)

Reprexain 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63717-902-01)
(Hawthorn Pharmaceuticals, Inc.)

NDC Code63717-902-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63717-902-01)
Product NDC63717-902
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
Strength10; 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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