# Hydroxyzine hydrochloride

NDC: 76420-883
Generic name: Hydroxyzine hydrochloride
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140820

FDA application: ANDA204279

## 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:"76420-883"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-883
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f3266f4-00a6-4c0c-bff2-e606913de894