NDC 55111-533
Divalproex Sodium 250 mg tablet, film coated, extended release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Recalls
- Jan 31, 2019 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications: Out of specification results observed for high dissolution.
Lots: Lot #: C802676, Exp 03/20 - May 22, 2015 · Class II · Dr. Reddy's Laboratories, Inc.
Failed Dissolution Specifications; exceeded specification at the 9 hour time point
Lots: 100 count bottle - Lot #C307859, exp 09/2015; 500 count bottle - Lot #C307859 and Lot# C307812, exp 09/2015
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA090161
- On the market since
- Aug 11, 2013
- Package NDCs
55111-533-0155111-533-0555111-533-3055111-533-6055111-533-7855111-533-79- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
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