# Meclizine Hydrochloride

NDC: 70710-1162
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201029

FDA application: ANDA213957

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=947a03c5-bca0-4d97-90b9-bcd6d6588273