# Fexofenadine hydrochloride

NDC: 10202-229
Generic name: Fexofenadine hydrochloride
Labeler / Manufacturer: 7-eleven
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150115

FDA application: ANDA202039

## 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:"10202-229"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10202-229
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d5914c05-e8db-4c79-82d0-a279d1304118