NDC 72162-1784

Mexiletine Hydrochloride 250 mg capsule

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-957.

United States: 1

Where the pills inside were 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

Repackaging site

Product details

Generic drug
Mexiletine: every company that makes it
Form
capsule, oral
Strength
250 mg
Approval
ANDA ANDA214089
On the market since
Nov 29, 2021
Package NDCs
72162-1784-1
Official label
DailyMed (National Library of Medicine), updated Oct 18, 2024

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