"63629-1469-0" National Drug Code (NDC)

Ibuprofen 21 TABLET in 1 BOTTLE (63629-1469-0)
(Bryant Ranch Prepack)

NDC Code63629-1469-0
Package Description21 TABLET in 1 BOTTLE (63629-1469-0)
Product NDC63629-1469
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20091123
Marketing Category NameANDA
Application NumberANDA078558
ManufacturerBryant Ranch Prepack
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesCyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

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