NDC 11673-571

up and up allergy relief

Fexofenadine Hydrochloride

up and up allergy relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Fexofenadine Hydrochloride.

Product ID11673-571_35fed2cb-b43d-4b0c-a50a-8b9e3a8cab9e
NDC11673-571
Product TypeHuman Otc Drug
Proprietary Nameup and up allergy relief
Generic NameFexofenadine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-04-13
Marketing CategoryANDA / ANDA
Application NumberANDA076447
Labeler NameTarget Corporation
Substance NameFEXOFENADINE HYDROCHLORIDE
Active Ingredient Strength180 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 11673-571-01

1 BOTTLE in 1 CARTON (11673-571-01) > 70 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2015-03-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-571-49 [11673057149]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-02-05

NDC 11673-571-39 [11673057139]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-04-13

NDC 11673-571-76 [11673057176]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-03-16

NDC 11673-571-95 [11673057195]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-11-02
Marketing End Date2016-08-18

NDC 11673-571-75 [11673057175]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-02-16
Marketing End Date2016-05-16

NDC 11673-571-22 [11673057122]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2011-04-26

NDC 11673-571-01 [11673057101]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-03-17

NDC 11673-571-87 [11673057187]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-03-15
Marketing End Date2018-07-31

NDC 11673-571-33 [11673057133]

up and up allergy relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076447
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-03-13

Drug Details

Active Ingredients

IngredientStrength
FEXOFENADINE HYDROCHLORIDE180 mg/1

OpenFDA Data

SPL SET ID:be80a7d9-e90b-460a-b72c-0ac60a75804b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 997420

    • NDC Crossover Matching brand name "up and up allergy relief" or generic name "Fexofenadine Hydrochloride"

    NDCBrand NameGeneric Name
    11673-462up and up allergy reliefdiphenhydramine hydrochloride
    11673-502Up and Up Allergy ReliefCetirizine Hydrochloride
    11673-571up and up allergy relieffexofenadine hydrochloride
    11673-612up and up allergy reliefLoratadine
    11673-617up and up allergy relieffexofenadine hydrochloride
    11673-690up and up allergy reliefDiphenhydramine Hydrochloride
    11673-705up and up allergy reliefcetirizine Hydrochloride
    11673-800up and up allergy reliefFexofenadine Hydrochloride
    10202-107AllergyFexofenadine hydrochloride
    11822-0425allergy relieffexofenadine hydrochloride
    11822-0571allergy relieffexofenadine hydrochloride
    0363-0095Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0097Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-0783Fexofenadine hydrochlorideFexofenadine hydrochloride
    0363-9898Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5619Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-5620Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0615-7636Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5961Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5962Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-5963Fexofenadine HydrochlorideFexofenadine Hydrochloride
    0904-6214fexofenadine hydrochloridefexofenadine hydrochloride
    0904-6711Fexofenadine hydrochlorideFexofenadine hydrochloride
    10202-229Fexofenadine hydrochlorideFexofenadine hydrochloride
    0179-8325Fexofenadine Hydrochloride 180Fexofenadine Hydrochloride
    0113-0571good sense aller easefexofenadine hydrochloride
    0113-0847good sense aller easefexofenadine hydrochloride
    0363-0571wal fex allergyfexofenadine hydrochloride
    0363-0784Wal-FexFexofenadine hydrochloride
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