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"11673-314-90" National Drug Code (NDC)

Up And Up Ibuprofen 500 TABLET, FILM COATED in 1 BOTTLE (11673-314-90)
(Target Corporation)

NDC Code11673-314-90
Package Description500 TABLET, FILM COATED in 1 BOTTLE (11673-314-90)
Product NDC11673-314
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Ibuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200313
Marketing Category NameANDA
Application NumberANDA072096
ManufacturerTarget Corporation
Substance NameIBUPROFEN
Strength200
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/11673-314-90





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