"61919-125-30" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BOTTLE (61919-125-30)
(Direct Rx)

NDC Code61919-125-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (61919-125-30)
Product NDC61919-125
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA078558
ManufacturerDirect Rx
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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