# HYDROXYZINE HYDROCHLORIDE

NDC: 83745-232
Generic name: HYDROXYZINE HYDROCHLORIDE
Labeler / Manufacturer: APOZEAL PHARMACEUTICALS INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20240716

FDA application: ANDA210634

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83745-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83745-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87d4bbff-0498-4c26-86cb-7ce173afa0b6