# Hydroxyzine Hydrochloride

NDC: 10702-012
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: KVK-Tech, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120724

FDA application: ANDA040786

## 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:"10702-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10702-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=adc4cb73-77c6-48ff-aaf2-b3568d53de1f