NDC 71335-3171
Mexiletine Hydrochloride 150 mg capsule
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-666.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zenara Pharma Private Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 21, 2024 · 1 inspection |
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 ANDA215315
- On the market since
- Feb 5, 2025
- Package NDCs
71335-3171-171335-3171-2- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?