# Hydroxyzine Hydrochloride

NDC: 72789-269
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: 20121022

FDA application: ANDA088619

## 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:"72789-269"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-269
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=214b3f14-2f6c-4f36-b7a6-e0b1f820e3a7