NDC 46708-821
Divalproex sodium 125 mg capsule, delayed release
On the label: Alembic Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 125 mg
- Approval
- ANDA ANDA218793
- On the market since
- Dec 23, 2024
- Package NDCs
46708-821-1046708-821-3146708-821-91- Official label
- DailyMed (National Library of Medicine), updated Jan 6, 2025
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