"61919-628-30" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BOTTLE (61919-628-30)
(DIRECT RX)

NDC Code61919-628-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-628-30)
Product NDC61919-628
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190329
Marketing Category NameANDA
Application NumberANDA091625
ManufacturerDIRECT RX
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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