"57664-102-88" National Drug Code (NDC)

Hydrocodone Bitartrate And Ibuprofen 100 TABLET, FILM COATED in 1 BOTTLE (57664-102-88)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-102-88
Package Description100 TABLET, FILM COATED in 1 BOTTLE (57664-102-88)
Product NDC57664-102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameHydrocodone Bitartrate And Ibuprofen
Non-Proprietary NameHydrocodone Bitartrate And Ibuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130528
Marketing Category NameANDA
Application NumberANDA091633
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameHYDROCODONE BITARTRATE; IBUPROFEN
Strength7.5; 200
Strength Unitmg/1; mg/1
Pharmacy ClassesOpioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
DEA ScheduleCII

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