# Hydroxyzine Hydrochloride

NDC: 0517-4201
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: American Regent, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 19900930

FDA application: ANDA087408

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0517-4201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0517-4201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8af7e5ce-d9d9-44cc-9f2f-4ddbc89e758a