NDC 53808-0831
Divalproex Sodium 500 mg tablet, film coated, extended release
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-0473.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 500 mg
- Approval
- ANDA ANDA077567
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0831-1- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2013
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