NDC 67046-138
Divalproex Sodium 500 mg tablet, delayed release
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 68382-033, made by Zydus Pharmaceuticals USA 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 (it lists 1 site that repackages it). 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 ANDA077100
- On the market since
- Sep 25, 2017
- Package NDCs
67046-138-0767046-138-1467046-138-1567046-138-2067046-138-2167046-138-2867046-138-3067046-138-60- Official label
- DailyMed (National Library of Medicine), updated Sep 25, 2017
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