NDC 82012-029

Mexiletine Hydrochloride 250 mg capsule

On the label: Senores Pharmaceuticals, Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Senores Pharmaceuticals, Inc. names for other drugs.

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
82012-029-04
Official label
DailyMed (National Library of Medicine), updated Jun 16, 2023

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