"52959-656-42" National Drug Code (NDC)

NDC Code	52959-656-42
Package Description	42 TABLET, FILM COATED in 1 BOTTLE (52959-656-42)
Product NDC	52959-656
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nabumetone
Non-Proprietary Name	Nabumetone
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20080301
Marketing Category Name	ANDA
Application Number	ANDA078671
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	NABUMETONE
Strength	750
Strength Unit	mg/1
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]