"30142-495-82" National Drug Code (NDC)

NDC Code	30142-495-82
Package Description	200 TABLET, FILM COATED in 1 BOTTLE (30142-495-82)
Product NDC	30142-495
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20150828
End Marketing Date	20230331
Marketing Category Name	ANDA
Application Number	ANDA072096
Manufacturer	Kroger Company
Substance Name	IBUPROFEN
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]