"70934-051-21" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-051-21)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-051-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-051-21)
Product NDC70934-051
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171212
End Marketing Date20231231
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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