# Childrens Allergy

NDC: 37808-623
Generic name: Fexofenadine HCL
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20210430
Marketing ended: 20270831
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:"37808-623"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-623
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b6f4a4b-b1bd-4062-9e7f-571b836b1536