fexofenadine hcl
Generic: fexofenadine hcl
Labeler: target corporationDrug Facts
Product Profile
Brand Name
fexofenadine hcl
Generic Name
fexofenadine hcl
Labeler
target corporation
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11673-767
Product ID
11673-767_46534182-fd58-f797-e063-6294a90a5106
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211075
Listing Expiration
2026-12-31
Marketing Start
2024-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673767
Hyphenated Format
11673-767
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
fexofenadine hcl (source: ndc)
Generic Name
fexofenadine hcl (source: ndc)
Application Number
ANDA211075 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (11673-767-03)
- 15 TABLET in 1 BLISTER PACK (11673-767-07)
- 150 TABLET in 1 BOTTLE (11673-767-15)
- 70 TABLET in 1 BOTTLE (11673-767-34)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46534182-fd58-f797-e063-6294a90a5106", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["fdb8451b-fba3-c7ca-e053-6294a90a05d7"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (11673-767-03)", "package_ndc": "11673-767-03", "marketing_start_date": "20240301"}, {"sample": false, "description": "15 TABLET in 1 BLISTER PACK (11673-767-07)", "package_ndc": "11673-767-07", "marketing_start_date": "20240301"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (11673-767-15)", "package_ndc": "11673-767-15", "marketing_start_date": "20240301"}, {"sample": false, "description": "70 TABLET in 1 BOTTLE (11673-767-34)", "package_ndc": "11673-767-34", "marketing_start_date": "20240301"}], "brand_name": "Fexofenadine HCL", "product_id": "11673-767_46534182-fd58-f797-e063-6294a90a5106", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11673-767", "generic_name": "Fexofenadine HCL", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine HCL", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}