# Allergy Relief

NDC: 83324-009
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: Chain Drug Marketing Association, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230522

FDA application: ANDA211075

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83324-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83324-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fabb8c0d-b4da-ab73-e053-6394a90ab8b5