# Meclizine Hydrochloride

NDC: 42806-014
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: Epic Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120430

FDA application: ANDA200294

## 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:"42806-014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=467e464b-bbaf-4053-9136-39e47a92fa05