# Allergy Relief

NDC: 54257-170
Generic name: FEXOFENADINE HYDROCHLORIDE
Labeler / Manufacturer: Magno-Humphries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210325

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:"54257-170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54257-170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f8a2f98-7eba-48df-9589-58587d67ae0e