NDC 70518-4553
divalproex sodium 500 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-381.
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 Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA214643
- On the market since
- Jan 21, 2026
- Package NDCs
70518-4553-0- Official label
- DailyMed (National Library of Medicine), updated Sep 16, 2026
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