# Hydroxyzine Hydrochloride

NDC: 69452-395
Generic name: Hydroxyzine Hydrochloride Oral
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250717

FDA application: ANDA219289

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-395"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-395
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=39f93633-000e-6c3f-e063-6394a90a5a0b