NDC 42291-625
Mexiletine Hydrochloride 200 mg capsule
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-8740.
Where the pills inside were 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Mexiletine: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA074377
- On the market since
- Jul 9, 2013
- Package NDCs
42291-625-01- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?