# Fexofenadine Hydrochloride

NDC: 68016-995
Generic name: Fexofenadine hydrochloride
Labeler / Manufacturer: Chain Drug Consortium, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140401

FDA application: ANDA076502

## 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:"68016-995"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-995
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1d8d0ec-2bdd-fb07-a051-d6353e3c240c