# Allergy Relief

NDC: 57344-292
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: AAA PHARMACEUTICAL, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210706

FDA application: ANDA211075

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57344-292"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57344-292
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c547c163-2a19-10d8-e053-2a95a90ac817