# Hydroxyzine Hydrochloride

NDC: 43063-518
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: ANDA040787

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-518"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-518
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24cb9c83-a7e4-4bae-997c-c3a87426f78c