"50436-0684-5" National Drug Code (NDC)

Ibu 12 TABLET in 1 BOTTLE (50436-0684-5)
(Unit Dose Services)

NDC Code50436-0684-5
Package Description12 TABLET in 1 BOTTLE (50436-0684-5)
Product NDC50436-0684
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerUnit Dose Services
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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