# Hydroxyzine Hydrochloride

NDC: 43063-960
Generic name: hydroxyzine hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, 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: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-960"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-960
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a3e389f-391d-4f37-9e34-ce3c6f5fe8c1