NDC 67046-121
Divalproex Sodium 500 mg tablet, delayed release
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 0245-0182, made by Upsher-Smith Laboratories, Inc. (Divalproex Sodium). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were 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 Coupler Enterprises Inc. names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release
- Strength
- 500 mg
- Approval
- ANDA ANDA078182
- On the market since
- Jul 29, 2008
- Package NDCs
67046-121-30- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2010
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