# MECLIZINE HYDROCHLORIDE

NDC: 51655-107
Generic name: MECLIZINE HYDROCHLORIDE
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140724
Marketing ended: 20261031
FDA application: ANDA040659

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-107"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-107
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c443873a-2e89-43b2-b145-dde3dadf7bc0