NDC 68151-2347
Mexiletine Hydrochloride 200 mg capsule
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management 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.
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Product details
- Generic drug
- Mexiletine: every company that makes it
- Form
- capsule
- Strength
- 200 mg
- Approval
- ANDA ANDA074377
- On the market since
- Jun 5, 1995
- Package NDCs
68151-2347-0- Official label
- DailyMed (National Library of Medicine), updated Jun 6, 2013
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