# FEXOFENADINE HYDROCHLORIDE

NDC: 72090-010
Generic name: FEXOFENADINE HYDROCHLORIDE
Labeler / Manufacturer: Pioneer Life Sciences, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231207

FDA application: ANDA210137

## 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:"72090-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72090-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7fe71e4-aada-40f5-86a8-bf0d7eb9b851