"0093-1016-10" National Drug Code (NDC)

Nabumetone 1000 TABLET, FILM COATED in 1 BOTTLE (0093-1016-10)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-1016-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0093-1016-10)
Product NDC0093-1016
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNabumetone
Non-Proprietary NameNabumetone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010926
End Marketing Date20180430
Marketing Category NameANDA
Application NumberANDA075189
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameNABUMETONE
Strength750
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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