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"11673-924-75" National Drug Code (NDC)

Dual Action Pain Relief 1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE
(TARGET CORPORATION)

NDC Code11673-924-75
Package Description1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE
Product NDC11673-924
Product Type NameHUMAN OTC DRUG
Proprietary NameDual Action Pain Relief
Non-Proprietary NameAcetaminophen, Ibuprofen
Dosage FormTABLET
UsageORAL
Start Marketing Date20230711
Marketing Category NameANDA
Application NumberANDA216994
ManufacturerTARGET CORPORATION
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-924-75





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