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"72189-643-21" National Drug Code (NDC)

Ibuprofen 21 TABLET, FILM COATED in 1 BOTTLE (72189-643-21)
(Direct_Rx)

NDC Code72189-643-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE (72189-643-21)
Product NDC72189-643
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250930
Marketing Category NameANDA
Application NumberANDA078329
ManufacturerDirect_Rx
Substance NameIBUPROFEN
Strength600
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/72189-643-21





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