"61919-123-28" National Drug Code (NDC)

NDC Code	61919-123-28
Package Description	28 TABLET, FILM COATED in 1 BOTTLE (61919-123-28)
Product NDC	61919-123
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Ibuprofen
Non-Proprietary Name	Ibuprofen
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20220510
End Marketing Date	20231027
Marketing Category Name	ANDA
Application Number	ANDA072096
Manufacturer	DirectRX
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]