"52959-076-04" National Drug Code (NDC)

NDC Code	52959-076-04
Package Description	4 TABLET in 1 BOTTLE (52959-076-04)
Product NDC	52959-076
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091123
Marketing Category Name	ANDA
Application Number	ANDA078558
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	IBUPROFEN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]