allegra allergy

Generic: fexofenadine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name allegra allergy
Generic Name fexofenadine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1234
Product ID 50090-1234_9840fda7-e713-4573-8029-046a50c67462
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA020872
Listing Expiration 2026-12-31
Marketing Start 2011-03-03

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 500901234
Hyphenated Format 50090-1234

Supplemental Identifiers

RxCUI
997420 997422 997501 997502
UNII
2S068B75ZU

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 allegra allergy (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number NDA020872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

50090-1234-0 1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

ALLEGRA ALLERGY ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9840fda7-e713-4573-8029-046a50c67462", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420", "997422", "997501", "997502"], "spl_set_id": ["b5ce28f8-f6c3-4113-9317-e1c98e5030ef"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50090-1234-0", "marketing_start_date": "20141128"}], "brand_name": "ALLEGRA ALLERGY", "product_id": "50090-1234_9840fda7-e713-4573-8029-046a50c67462", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50090-1234", "generic_name": "fexofenadine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALLEGRA ALLERGY", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "NDA020872", "marketing_category": "NDA", "marketing_start_date": "20110303", "listing_expiration_date": "20261231"}