"42291-339-50" National Drug Code (NDC)

Ibuprofen 500 TABLET in 1 BOTTLE (42291-339-50)
(AvKARE, Inc.)

NDC Code42291-339-50
Package Description500 TABLET in 1 BOTTLE (42291-339-50)
Product NDC42291-339
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20130124
Marketing Category NameANDA
Application NumberANDA078558
ManufacturerAvKARE, Inc.
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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