# Allergy Relief

NDC: 68016-887
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: CHAIN DRUG CONSORTIUM
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210708
Marketing ended: 20260930
FDA application: ANDA211075

## 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:"68016-887"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-887
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8eee26c2-af58-469c-b855-c3bfc8bd7e2d