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"11673-571-22" National Drug Code (NDC)

Up And Up Allergy Relief 15 BLISTER PACK in 1 CARTON (11673-571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(Target Corporation)

NDC Code11673-571-22
Package Description15 BLISTER PACK in 1 CARTON (11673-571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC11673-571
Product Type NameHUMAN OTC DRUG
Proprietary NameUp And Up Allergy Relief
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110413
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerTarget Corporation
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11673-571-22





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