# Fexofenadine HCL

NDC: 71205-531
Generic name: Fexofenadine HCL
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160819

FDA application: ANDA204097

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-531"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-531
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f9a7e836-6055-484f-a197-181220428574
