# Fexofenadine Hydrochloride

NDC: 51655-231
Generic name: Fexofenadine HCl
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20221116
Marketing ended: 20261028
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:"51655-231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2b6c157-1af1-8d43-e053-2995a90aaf1a