# Childrens Allergy

NDC: 61269-527
Generic name: fexofenadine hydrochloride
Labeler / Manufacturer: H2-Pharma, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20220718

FDA application: ANDA203330

## 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:"61269-527"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61269-527
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=84988f6d-85b1-45dd-89be-0333acc6b180