# MECLIZINE HYDROCHLORIDE

NDC: 59746-122
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: Jubilant Cadista Pharmacuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100604
Marketing ended: 20261031
FDA application: ANDA040659

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 12.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59746-122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59746-122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9350fefc-9c00-182c-c3a9-044d4a40856f