"61919-463-21" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (61919-463-21)
(Direct_Rx)

NDC Code61919-463-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (61919-463-21)
Product NDC61919-463
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuorofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190822
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerDirect_Rx
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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