"0093-1016-01" National Drug Code (NDC)

NDC Code	0093-1016-01
Package Description	100 TABLET, FILM COATED in 1 BOTTLE (0093-1016-01)
Product NDC	0093-1016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nabumetone
Non-Proprietary Name	Nabumetone
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20010926
End Marketing Date	20180430
Marketing Category Name	ANDA
Application Number	ANDA075189
Manufacturer	Teva Pharmaceuticals USA, 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]