NDC 0143-9637
Valproate Sodium 100 mg per 1 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
- 100 mg per 1 mL
- Approval
- ANDA ANDA078523
- On the market since
- Apr 15, 2013
- Package NDCs
0143-9637-010143-9637-10- Official label
- DailyMed (National Library of Medicine), updated Nov 20, 2023
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