"68071-2789-3" National Drug Code (NDC)

Ibuprofen 30 TABLET, FILM COATED in 1 BOTTLE (68071-2789-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2789-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-2789-3)
Product NDC68071-2789
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211021
Marketing Category NameANDA
Application NumberANDA071268
ManufacturerNuCare Pharmaceuticals,Inc.
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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