# allergy relief

NDC: 79481-0847
Generic name: fexofenadine hydrochloride
Labeler / Manufacturer: Meijer, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211006

FDA application: ANDA212971

## 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:"79481-0847"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79481-0847
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=deecbf76-be1d-4b27-85c6-17cfb7e7d1a1