# Fexofenadine Hydrochloride

NDC: 84324-045
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: NUVICARE LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260730

FDA application: ANDA204507

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 60 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84324-045"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84324-045
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd0da52b-fc82-4ec9-854c-0d7c52e926fb