# MEXILETINE HYDROCHLORIDE

NDC: 72162-1784
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: 20211129

FDA application: ANDA214089

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0ff45dbf-b555-4f55-a286-98bfaea9ea29