NDC 0143-9785
Valproate Sodium 500 mg per 5 mL injection
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- injection, intravenous
- Strength
- 500 mg per 5 mL
- Approval
- ANDA ANDA078523
- On the market since
- Feb 17, 2010
- Package NDCs
0143-9785-010143-9785-10- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2023
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