NDC 62756-955

Mexiletine Hydrochloride 150 mg capsule

On the label: Caraco Pharmaceutical Laboratories, Ltd..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Havix Group Inc d/b/a Aavis PharmaceuticalsHoschton, GA, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJul 25, 2025 · 2 inspections

Product details

Generic drug
Mexiletine: every company that makes it
Form
capsule, oral
Strength
150 mg
Approval
ANDA ANDA214089
On the market since
Nov 29, 2021
Package NDCs
62756-955-01
Official label
DailyMed (National Library of Medicine), updated Apr 27, 2023

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