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"71205-604-21" National Drug Code (NDC)

Ibu 21 TABLET in 1 BOTTLE (71205-604-21)
(Proficient Rx LP)

NDC Code71205-604-21
Package Description21 TABLET in 1 BOTTLE (71205-604-21)
Product NDC71205-604
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbu
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20081120
Marketing Category NameANDA
Application NumberANDA075682
ManufacturerProficient Rx LP
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/71205-604-21





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