"0093-0711-05" National Drug Code (NDC)

Flurbiprofen 500 TABLET, FILM COATED in 1 BOTTLE (0093-0711-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0711-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (0093-0711-05)
Product NDC0093-0711
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFlurbiprofen
Non-Proprietary NameFlurbiprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19950602
Marketing Category NameANDA
Application NumberANDA074431
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameFLURBIPROFEN
Strength100
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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