"70518-3830-0" National Drug Code (NDC)

Nabumetone 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3830-0)
(REMEDYREPACK INC.)

NDC Code70518-3830-0
Package Description14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3830-0)
Product NDC70518-3830
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNabumetone
Non-Proprietary NameNabumetone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230815
Marketing Category NameANDA
Application NumberANDA078671
ManufacturerREMEDYREPACK INC.
Substance NameNABUMETONE
Strength500
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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