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"68084-922-32" National Drug Code (NDC)

Nabumetone 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-922-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-922-33)
(American Health Packaging)

NDC Code68084-922-32
Package Description20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-922-32) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-922-33)
Product NDC68084-922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNabumetone
Non-Proprietary NameNabumetone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150331
Marketing Category NameANDA
Application NumberANDA091083
ManufacturerAmerican Health Packaging
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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