NDC 33261-621
Divalproex SodiumDelayed-ReleaseDelayed-Release 500 mg tablet, film coated
On the label: Aidarex Pharmaceuticals LLC. It's repackaged from NDC 0603-3443, made by Qualitest Pharmaceuticals (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 Aidarex Pharmaceuticals LLC names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA090210
- On the market since
- Nov 30, 2009
- Package NDCs
33261-621-60- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2013
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