NDC 70771-1742
vigabatrin 500 mg per 10 mL powder, for solution
On the label: Cadila Healthcare Limited.
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
70771-1742-170771-1742-8- Official label
- DailyMed (National Library of Medicine), updated Nov 7, 2025
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