"69452-447-22" National Drug Code (NDC)

Dual Action Pain Reliever 1 BOTTLE in 1 CARTON (69452-447-22) / 120 TABLET, FILM COATED in 1 BOTTLE
(Bionpharma Inc.)

NDC Code69452-447-22
Package Description1 BOTTLE in 1 CARTON (69452-447-22) / 120 TABLET, FILM COATED in 1 BOTTLE
Product NDC69452-447
Product Type NameHUMAN OTC DRUG
Proprietary NameDual Action Pain Reliever
Non-Proprietary NameAcetaminophen And Ibuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240808
Marketing Category NameANDA
Application NumberANDA216999
ManufacturerBionpharma Inc.
Substance NameACETAMINOPHEN; IBUPROFEN
Strength250; 125
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

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