# Mexiletine Hydrochloride

NDC: 72162-1773
Generic name: Mexiletine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200622

FDA application: ANDA074450

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1773"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1773
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0bd3f2c-44e5-4ad0-9b76-c2028f0cae11