# Allergy Relief

NDC: 59726-801
Generic name: Fexofenadine HCl
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20210820
Marketing ended: 20261230
FDA application: ANDA204507

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59726-801"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-801
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a976ad95-33d2-49f5-bad5-e980bf764879