allergy relief

Generic: fexofenadine hydrochloride

Labeler: heb
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler heb
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 60 mg/1

Manufacturer
HEB

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808391
Hyphenated Format 37808-391

Supplemental Identifiers

RxCUI
997501
UPC
0041220853632
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 ANDA211075 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (37808-391-02) / 12 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

fexofenadine hydrochloride (60 mg/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"}