# Allergy Relief

NDC: 63548-0664
Generic name: Fexofenadine HCl
Labeler / Manufacturer: PLD Acquisitions LLC DBA Avma Pharma Solutions
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191001

FDA application: ANDA204097

## 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:"63548-0664"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63548-0664
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f1f292d-6d5f-4600-ad27-323e498ddecb