# Hydroxyzine Hydrochloride

NDC: 72162-2513
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211007

FDA application: ANDA087871

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-2513"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2513
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8c83479-f919-49f9-b125-747bd0e3211c