# Childrens Fexofenadine Hydrochloride Allergy

NDC: 0363-2141
Generic name: Fexofenadine Hydrochloride
Labeler / Manufacturer: Walgreens Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20241206

FDA application: ANDA208123

## 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:"0363-2141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-2141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=374f9271-b65b-69a9-e063-6394a90af36a