"61919-960-90" National Drug Code (NDC)

Ibuprofen 90 TABLET in 1 BOTTLE (61919-960-90)
(DirectRX)

NDC Code61919-960-90
Package Description90 TABLET in 1 BOTTLE (61919-960-90)
Product NDC61919-960
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerDirectRX
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

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