# HYDROXYZINE HYDROCHLORIDE

NDC: 70518-4141
Generic name: hydroxyzine hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240716

FDA application: ANDA217652

## 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:"70518-4141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f41912e-12ce-4174-a0fb-cfb4888d8d58