NDC 0121-1350
Valproic Acid 500 mg per 10 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- solution, oral
- Strength
- 500 mg per 10 mL
- Approval
- ANDA ANDA075379
- On the market since
- Apr 11, 2005
- Package NDCs
0121-1350-000121-1350-10- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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