NDC 58118-8814
Lacosamide 150 mg tablet, film coated
On the label: Clinical Solutions Wholesale. It's repackaged: Clinical Solutions Wholesale rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-814.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Repackaging site
- Clinical Solutions Wholesale, LLC, Franklin, TN, United States · repackages it
Recalls
- Jun 4, 2026 · Class II · Annora Pharma Private Limited
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
Lots: Lot: A253999, A254000, Expires: 09/30/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lacosamide: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA204787
- On the market since
- Mar 17, 2022
- Package NDCs
58118-8814-8- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
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