"52959-245-20" National Drug Code (NDC)

NDC Code	52959-245-20
Package Description	20 CAPSULE in 1 BOTTLE (52959-245-20)
Product NDC	52959-245
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ketoprofen
Non-Proprietary Name	Ketoprofen
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20110118
Marketing Category Name	ANDA
Application Number	ANDA073516
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	KETOPROFEN
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]