NDC 70518-3457
Divalproex sodium 125 mg capsule, coated pellets
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-115.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- capsule, coated pellets, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA213181
- On the market since
- Aug 1, 2023
- Package NDCs
70518-3457-070518-3457-170518-3457-270518-3457-370518-3457-4- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2026
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