"52125-780-02" National Drug Code (NDC)

NDC Code	52125-780-02
Package Description	30 TABLET in 1 BLISTER PACK (52125-780-02)
Product NDC	52125-780
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20131111
End Marketing Date	20171005
Marketing Category Name	ANDA
Application Number	ANDA090796
Manufacturer	REMEDYREPACK 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]