# FEXOFENADINE HYDROCHLORIDE

NDC: 46122-779
Generic name: FEXOFENADINE HYDROCHLORIDE
Labeler / Manufacturer: AMERISOURCE BERGEN
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240514

FDA application: ANDA091567

## 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:"46122-779"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-779
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a578643-adc1-44ca-83f2-9d48527bd3a4