allergy relief

Generic: fexofenadine hydrochloride

Labeler: retail business services , llc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler retail business services , llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
RETAIL BUSINESS SERVICES , LLC.

Identifiers & Regulatory

Product NDC 72476-192
Product ID 72476-192_cf22d677-c125-1721-e053-2a95a90a1c3e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211075
Listing Expiration 2026-12-31
Marketing Start 2021-07-14

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 72476192
Hyphenated Format 72476-192

Supplemental Identifiers

RxCUI
997420
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
  • 180 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-04) / 30 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-06) / 45 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-09) / 90 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (3)

72476-192-04 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-04) / 30 TABLET in 1 BOTTLE, PLASTIC 72476-192-06 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-06) / 45 TABLET in 1 BOTTLE, PLASTIC 72476-192-09 1 BOTTLE, PLASTIC in 1 CARTON (72476-192-09) / 90 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

fexofenadine hydrochloride (180 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": "cf22d677-c125-1721-e053-2a95a90a1c3e", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c1be67ea-9973-49e2-e053-2995a90a423c"], "manufacturer_name": ["RETAIL BUSINESS SERVICES , LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-192-04)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "72476-192-04", "marketing_start_date": "20211004"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-192-06)  / 45 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "72476-192-06", "marketing_start_date": "20211004"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-192-09)  / 90 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "72476-192-09", "marketing_start_date": "20210714"}], "brand_name": "ALLERGY RELIEF", "product_id": "72476-192_cf22d677-c125-1721-e053-2a95a90a1c3e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72476-192", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "RETAIL BUSINESS SERVICES , LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLERGY RELIEF", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20210714", "listing_expiration_date": "20261231"}