# MEXILETINE HYDROCHLORIDE

NDC: 50742-241
Generic name: Mexiletine hydrochloride
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20210126

FDA application: ANDA214352

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-241"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-241
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6dbf86f7-2b2d-40fb-868b-ee7d7a95556e