NDC 70710-1494
vigabatrin 500 mg per 10 mL powder, for solution
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Vigabatrin: every company that makes it
- Form
- powder, for solution, oral
- Strength
- 500 mg per 10 mL
- Approval
- ANDA ANDA214671
- On the market since
- Mar 24, 2025
- Package NDCs
70710-1494-170710-1494-8- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2024
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