allergy relief
Generic: fexofenadine hydrochloride
Labeler: safeway incDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
fexofenadine hydrochloride
Labeler
safeway inc
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 180 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
21130-784
Product ID
21130-784_763513d2-273c-404d-8f8f-6df12b44fc6b
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076502
Listing Expiration
2026-12-31
Marketing Start
2013-04-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
21130784
Hyphenated Format
21130-784
Supplemental Identifiers
RxCUI
UNII
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
ANDA076502 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 180 mg/1
Packaging
- 3 BLISTER PACK in 1 CARTON (21130-784-29) / 5 TABLET in 1 BLISTER PACK
- 1 BOTTLE in 1 CARTON (21130-784-30) / 30 TABLET in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "763513d2-273c-404d-8f8f-6df12b44fc6b", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["3c30a1dc-a13d-2522-d4d0-00c1e9dbab07"], "manufacturer_name": ["Safeway Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (21130-784-29) / 5 TABLET in 1 BLISTER PACK", "package_ndc": "21130-784-29", "marketing_start_date": "20130422"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (21130-784-30) / 30 TABLET in 1 BOTTLE", "package_ndc": "21130-784-30", "marketing_start_date": "20130422"}], "brand_name": "Allergy Relief", "product_id": "21130-784_763513d2-273c-404d-8f8f-6df12b44fc6b", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "21130-784", "generic_name": "Fexofenadine hydrochloride", "labeler_name": "Safeway Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA076502", "marketing_category": "ANDA", "marketing_start_date": "20130422", "listing_expiration_date": "20261231"}