allergy relief

Generic: fexofenadine hydrochloride

Labeler: yyba corp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fexofenadine hydrochloride 60 mg/1

Manufacturer
YYBA CORP

Identifiers & Regulatory

Product NDC 73581-103
Product ID 73581-103_4482573c-af39-436a-e063-6294a90ac4ea
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204507
Listing Expiration 2026-12-31
Marketing Start 2020-06-30

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 73581103
Hyphenated Format 73581-103

Supplemental Identifiers

RxCUI
997501
UPC
0373581000272 0373581000616 0373581103102
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 ANDA204507 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (73581-103-01)
  • 1 BOTTLE in 1 BOX (73581-103-10) / 100 TABLET in 1 BOTTLE
  • 200 TABLET in 1 BOTTLE (73581-103-20)
  • 60 TABLET in 1 BOTTLE (73581-103-60)
source: ndc

Packages (4)

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": "4482573c-af39-436a-e063-6294a90ac4ea", "openfda": {"upc": ["0373581000272", "0373581000616", "0373581103102"], "unii": ["2S068B75ZU"], "rxcui": ["997501"], "spl_set_id": ["a1e80757-346f-4d88-8da7-55583c3a902b"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (73581-103-01)", "package_ndc": "73581-103-01", "marketing_start_date": "20251127"}, {"sample": false, "description": "1 BOTTLE in 1 BOX (73581-103-10)  / 100 TABLET in 1 BOTTLE", "package_ndc": "73581-103-10", "marketing_start_date": "20200630"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (73581-103-20)", "package_ndc": "73581-103-20", "marketing_start_date": "20230606"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (73581-103-60)", "package_ndc": "73581-103-60", "marketing_start_date": "20250102"}], "brand_name": "ALLERGY RELIEF", "product_id": "73581-103_4482573c-af39-436a-e063-6294a90ac4ea", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73581-103", "generic_name": "FEXOFENADINE HYDROCHLORIDE", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLERGY RELIEF", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA204507", "marketing_category": "ANDA", "marketing_start_date": "20200630", "listing_expiration_date": "20261231"}