# HydrOXYzine Hydrochloride

NDC: 16714-082
Generic name: HydrOXYzine Hydrochloride
Labeler / Manufacturer: Northstar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091111

FDA application: ANDA040840

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16714-082"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-082
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8e5fce17-936e-46ea-a969-518c952c2091