allergy relief
Generic: fexofenadine hydrochloride
Labeler: hebDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
fexofenadine hydrochloride
Labeler
heb
Dosage Form
TABLET
Routes
Active Ingredients
fexofenadine hydrochloride 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-391
Product ID
37808-391_e051ce8b-3163-69b9-e053-2a95a90ab739
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211075
Listing Expiration
2026-12-31
Marketing Start
2022-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808391
Hyphenated Format
37808-391
Supplemental Identifiers
RxCUI
UPC
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
allergy relief (source: ndc)
Generic Name
fexofenadine hydrochloride (source: ndc)
Application Number
ANDA211075 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (37808-391-02) / 12 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e051ce8b-3163-69b9-e053-2a95a90ab739", "openfda": {"upc": ["0041220853632"], "unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["7cb25829-3aee-4a82-869d-ab4259626584"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (37808-391-02) / 12 TABLET in 1 BLISTER PACK", "package_ndc": "37808-391-02", "marketing_start_date": "20220531"}], "brand_name": "Allergy Relief", "product_id": "37808-391_e051ce8b-3163-69b9-e053-2a95a90ab739", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-391", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20220531", "listing_expiration_date": "20261231"}