# Hydroxyzine Hydrochloride

NDC: 60687-875
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250911

FDA application: ANDA087871

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-875"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-875
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fc148d96-b868-4e45-b7d2-977faf431049