# Meclizine Hydrochloride

NDC: 62135-954
Generic name: Meclizine Hydrochloride
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220811

FDA application: ANDA203003

## Active ingredients

- MECLIZINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62135-954"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-954
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87d4c6d8-9218-48c2-9163-615a32449f11