# FEXOFENADINE HYDROCHLORIDE

NDC: 84324-008
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: 20240717

FDA application: ANDA210137

## 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:"84324-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84324-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb47b839-3f49-4818-a62c-b6d2b09b15dc