allergy relief

Generic: fexofenadine hydrochloride

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-1847
Product ID 0363-1847_750c2665-b051-4585-94d7-70a9671796d2
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA212971
Listing Expiration 2026-12-31
Marketing Start 2024-02-01

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03631847
Hyphenated Format 0363-1847

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allergy relief (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA212971 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-1847-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1847-49) / 40 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1847-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1847-95) / 45 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (4)

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "750c2665-b051-4585-94d7-70a9671796d2", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["99f03481-d169-4aac-8370-20011ff530ea"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1847-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1847-39", "marketing_start_date": "20240201"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1847-49)  / 40 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1847-49", "marketing_start_date": "20241213"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1847-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1847-75", "marketing_start_date": "20240201"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1847-95)  / 45 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-1847-95", "marketing_start_date": "20240201"}], "brand_name": "Allergy Relief", "product_id": "0363-1847_750c2665-b051-4585-94d7-70a9671796d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-1847", "generic_name": "fexofenadine hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA212971", "marketing_category": "ANDA", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}