NDC 0363-0904

Indoor Outdoor Allergy Relief

Fexofenadine Hcl

Indoor Outdoor Allergy Relief is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is Fexofenadine Hydrochloride.

Product ID0363-0904_4e34e403-d23b-4da2-bbd0-f60c69d0aac8
NDC0363-0904
Product TypeHuman Otc Drug
Proprietary NameIndoor Outdoor Allergy Relief
Generic NameFexofenadine Hcl
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2018-08-31
Marketing CategoryANDA / ANDA
Application NumberANDA204507
Labeler NameWalgreens
Substance NameFEXOFENADINE HYDROCHLORIDE
Active Ingredient Strength180 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0363-0904-05

5 BLISTER PACK in 1 CARTON (0363-0904-05) > 1 TABLET, COATED in 1 BLISTER PACK
Marketing Start Date2018-08-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0904-90 [00363090490]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-15 [00363090415]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-05 [00363090405]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-70 [00363090470]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-45 [00363090445]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-30 [00363090430]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

NDC 0363-0904-51 [00363090451]

Indoor Outdoor Allergy Relief TABLET, COATED
Marketing CategoryANDA
Application NumberANDA204507
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-31

Drug Details

Active Ingredients

IngredientStrength
FEXOFENADINE HYDROCHLORIDE180 mg/1

OpenFDA Data

SPL SET ID:76159273-b46e-42b4-9418-173c86be1112
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 997420

    • NDC Crossover Matching brand name "Indoor Outdoor Allergy Relief" or generic name "Fexofenadine Hcl"

    NDCBrand NameGeneric Name
    0363-0858Indoor Outdoor Allergy ReliefLoratadine
    0363-0904Indoor Outdoor Allergy ReliefFexofenadine HCl
    10202-5717 Select Allergy Relieffexofenadine hcl
    0363-8010Allergy ReliefFexofenadine HCl
    0904-6978Allergy ReliefFexofenadine HCL
    0113-7425basic care allergyFexofenadine HCl
    0113-7571basic care allergyfexofenadine hcl
    0363-9230Dye Free Wal FexFexofenadine HCL
    0904-7192fexofenadine hclfexofenadine hcl
    0904-6979Fexofenadine HydrochlorideFexofenadine HCl
    0904-7050Fexofenadine HydrochlorideFexofenadine HCl
    10544-231Fexofenadine HydrochlorideFexofenadine HCl
    0113-0425Good Sense Aller EaseFexofenadine HCl
    0536-1066rugby fexofenadine hydrochloridefexofenadine hcl
    0363-0903Wal FexFexofenadine HCl
    0363-0600Wal Fex 24 Hour Allergyfexofenadine hcl
    0363-0425Wal fex AllergyFexofenadine HCl
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