"72189-231-21" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
(DIRECT RX)

NDC Code72189-231-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
Product NDC72189-231
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210604
Marketing Category NameANDA
Application NumberANDA090796
ManufacturerDIRECT RX
Substance NameIBUPROFEN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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