"68071-3125-1" National Drug Code (NDC)

Ibu 21 TABLET in 1 BOTTLE (68071-3125-1)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-3125-1
Package Description21 TABLET in 1 BOTTLE (68071-3125-1)
Product NDC68071-3125
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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