"61919-621-72" National Drug Code (NDC)

Ibuprofen 120 TABLET in 1 BOTTLE (61919-621-72)
(Direct_Rx)

NDC Code61919-621-72
Package Description120 TABLET in 1 BOTTLE (61919-621-72)
Product NDC61919-621
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20190820
Marketing Category NameANDA
Application NumberANDA075682
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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