NDC 53808-1061
Divalproex Sodium Extended-Release 500 mg tablet, extended release
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 68382-315, 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, extended release
- Strength
- 500 mg
- Approval
- NDA AUTHORIZED GENERIC NDA021168
- On the market since
- Nov 1, 2014
- Package NDCs
53808-1061-1- Official label
- DailyMed (National Library of Medicine), updated Jan 3, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?