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"11673-212-55" National Drug Code (NDC)

Up And Up Omeprazole 3 CARTON in 1 CARTON (11673-212-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
(Target Corporation)

NDC Code11673-212-55
Package Description3 CARTON in 1 CARTON (11673-212-55) > 14 BLISTER PACK in 1 CARTON > 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
Product NDC11673-212
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Omeprazole
Non-Proprietary NameOmeprazole
Dosage FormTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE
UsageORAL
Start Marketing Date20180509
Marketing Category NameNDA
Application NumberNDA209400
ManufacturerTarget Corporation
Substance NameOMEPRAZOLE
Strength20
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-212-55





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