# Fexofenadine Hydrochloride

NDC: 68210-2210
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: SPIRIT PHARMACEUTICALS LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200317

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:"68210-2210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68210-2210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae0f16f6-d07a-47e1-adb8-07803c6cfb13