NDC 50742-239

Mexiletine Hydrochloride 150 mg capsule

On the label: Ingenus Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ingenus Pharmaceuticals NJ, LLCFairfield, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundJan 9, 2026 · 11 inspections

Product details

Generic drug
Mexiletine: every company that makes it
Form
capsule, oral
Strength
150 mg
Approval
ANDA ANDA214352
On the market since
Jan 26, 2021
Package NDCs
50742-239-01
Official label
DailyMed (National Library of Medicine), updated Jul 28, 2023

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