# Fexofenadine HCl

NDC: 80513-506
Generic name: Fexofenadine HCl
Labeler / Manufacturer: Advanced Rx LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150916

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:"80513-506"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80513-506
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c067b335-79c5-4176-a0b3-bae02a0c23f8