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"61919-125-60" National Drug Code (NDC)

Ibuprofen 60 BOTTLE in 1 BOTTLE (61919-125-60) > 30 BOTTLE in 1 BOTTLE (61919-125-30) > 20 TABLET, FILM COATED in 1 BOTTLE (61919-125-20)
(Direct Rx)

NDC Code61919-125-60
Package Description60 BOTTLE in 1 BOTTLE (61919-125-60) > 30 BOTTLE in 1 BOTTLE (61919-125-30) > 20 TABLET, FILM COATED in 1 BOTTLE (61919-125-20)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-125-60





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