# Hydroxyzine Hydrochloride

NDC: 24658-783
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210721

FDA application: ANDA040604

## 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:"24658-783"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-783
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19fe26a9-eb1a-4c5b-a5e4-65223ee56ad1