# MECLIZINE HYDROCHLORIDE

NDC: 68788-4170
Generic name: MECLIZINE
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260803

FDA application: ANDA202640

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-4170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-4170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f755f8f3-7645-433c-b502-c1f15b700299