"52959-800-21" National Drug Code (NDC)

NDC Code	52959-800-21
Package Description	21 TABLET, FILM COATED in 1 BOTTLE (52959-800-21)
Product NDC	52959-800
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Oxaprozin
Non-Proprietary Name	Oxaprozin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20010131
Marketing Category Name	ANDA
Application Number	ANDA075855
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	OXAPROZIN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]