NDC 71335-2922
Mexiletine Hydrochloride 150 mg capsule
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-955.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Havix Group Inc d/b/a Aavis Pharmaceuticals | Hoschton, GA, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 25, 2025 · 2 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Mexiletine: every company that makes it
- Form
- capsule, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA214089
- On the market since
- Nov 29, 2021
- Package NDCs
71335-2922-1- Official label
- DailyMed (National Library of Medicine), updated Nov 6, 2025
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