# MEXILETINE HYDROCHLORIDE

NDC: 82012-027
Generic name: mexiletine hydrochloride
Labeler / Manufacturer: Senores Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20200307

FDA application: ANDA202111

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82012-027"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82012-027
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4a60f9e-fed1-4172-adc4-0be84ac65db9