allergy relief

Generic: fexofenadine hydrochloride

Labeler: chain drug marketing association, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler chain drug marketing association, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 60 mg/1

Manufacturer
Chain Drug Marketing Association, Inc.

Identifiers & Regulatory

Product NDC 83324-009
Product ID 83324-009_fc49fe88-56a3-6dcf-e053-6294a90adb84
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211075
Listing Expiration 2026-12-31
Marketing Start 2023-05-22

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 83324009
Hyphenated Format 83324-009

Supplemental Identifiers

RxCUI
997501
UPC
0635515998568
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 (83324-009-12) / 12 TABLET in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (83324-009-24) / 12 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

83324-009-12 1 BLISTER PACK in 1 CARTON (83324-009-12) / 12 TABLET in 1 BLISTER PACK 83324-009-24 2 BLISTER PACK in 1 CARTON (83324-009-24) / 12 TABLET in 1 BLISTER PACK

Ingredients (1)

fexofenadine hydrochloride (60 mg/1)

Linked Drug Pages (1)

Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc49fe88-56a3-6dcf-e053-6294a90adb84", "openfda": {"upc": ["0635515998568"], "unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["fabb8c0d-b4da-ab73-e053-6394a90ab8b5"], "manufacturer_name": ["Chain Drug Marketing Association, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (83324-009-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "83324-009-12", "marketing_start_date": "20230522"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (83324-009-24)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "83324-009-24", "marketing_start_date": "20230522"}], "brand_name": "Allergy Relief", "product_id": "83324-009_fc49fe88-56a3-6dcf-e053-6294a90adb84", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83324-009", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "Chain Drug Marketing Association, Inc.", "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": "20230522", "listing_expiration_date": "20261231"}