# Hydroxyzine Hydrochloride

NDC: 65162-577
Generic name: Hydroxyzine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20080924

FDA application: ANDA040808

## 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:"65162-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=89901966-724b-4773-98b8-ea663ceabd53