# Hydroxyzine hydrochloride

NDC: 63187-354
Generic name: Hydroxyzine hydrochloride
Labeler / Manufacturer: Proficient Rx LP
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:"63187-354"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-354
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=73993c7e-acd7-4835-be03-f8274a15955b
