# FEXOFENADINE HYDROCHLORIDE

NDC: 51316-800
Generic name: FEXOFENADINE HYDROCHLORIDE
Labeler / Manufacturer: CVS PHARMACY, INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220920

FDA application: ANDA091567

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 180 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51316-800"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51316-800
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7bc13851-291a-4582-8261-13c5022fbdd1