NDC 55111-531
divalproex sodium 500 mg tablet, delayed release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Dr.Reddy's Laboratories Ltd. names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA078755
- On the market since
- Jul 29, 2008
- Package NDCs
55111-531-0155111-531-0555111-531-3055111-531-7855111-531-79- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2018
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