non-drowsy allergy relief

Generic: fexofenadine hydrochloride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name non-drowsy allergy relief
Generic Name fexofenadine hydrochloride
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-621
Product ID 11673-621_d7eb1caf-eeff-10b7-c464-3592c8d7d0ee
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA076502
Listing Expiration 2026-12-31
Marketing Start 2025-08-01

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 11673621
Hyphenated Format 11673-621

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

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 non-drowsy allergy relief (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA076502 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-621-01) / 150 TABLET in 1 BOTTLE
  • 3 BLISTER PACK in 1 CARTON (11673-621-15) / 5 TABLET in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (11673-621-30) / 30 TABLET in 1 BOTTLE
  • 150 TABLET in 1 BOTTLE (11673-621-50)
  • 1 BOTTLE in 1 CARTON (11673-621-70) / 70 TABLET in 1 BOTTLE
source: ndc

Packages (5)

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": "d7eb1caf-eeff-10b7-c464-3592c8d7d0ee", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["3cf4b7fe-b1f7-b767-430a-655408f91753"], "manufacturer_name": ["TARGET CORPORATION"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-621-01)  / 150 TABLET in 1 BOTTLE", "package_ndc": "11673-621-01", "marketing_start_date": "20250801"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (11673-621-15)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "11673-621-15", "marketing_start_date": "20250801"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-621-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "11673-621-30", "marketing_start_date": "20250801"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (11673-621-50)", "package_ndc": "11673-621-50", "marketing_start_date": "20250801"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-621-70)  / 70 TABLET in 1 BOTTLE", "package_ndc": "11673-621-70", "marketing_start_date": "20250801"}], "brand_name": "Non-Drowsy Allergy Relief", "product_id": "11673-621_d7eb1caf-eeff-10b7-c464-3592c8d7d0ee", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11673-621", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Non-Drowsy Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}