# MECLIZINE HYDROCHLORIDE

NDC: 63629-2432
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
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:"63629-2432"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2432
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c66ee38-10bb-4559-9d2f-51e6d6f091ee