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"68071-3172-2" National Drug Code (NDC)

Ibu 20 TABLET in 1 BOTTLE (68071-3172-2)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-3172-2
Package Description20 TABLET in 1 BOTTLE (68071-3172-2)
Product NDC68071-3172
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
Strength400
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-3172-2





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