# Mexiletine hydrochloride

NDC: 31722-037
Generic name: Mexiletine hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20221109

FDA application: ANDA216463

## Active ingredients

- MEXILETINE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8b20e850-037b-4c16-a57d-c3d4909f147a