# Fexofenadine Hydrochloride

NDC: 58602-426
Generic name: Fexofenadine Hydrochloride Oral
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20230523

FDA application: ANDA213466

## Active ingredients

- FEXOFENADINE HYDROCHLORIDE: 30 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-426"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-426
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8e35d7a-a86b-4d37-979b-f454978f070b