# Meclizine Hydrochloride

NDC: 51655-175
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: 20221007

FDA application: ANDA201451

## 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:"51655-175"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-175
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2b4716c-411a-62cd-e053-2a95a90a6f4b