NDC 53808-1027
Divalproex Sodium 250 mg tablet, delayed release
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 0245-0181, made by Upsher-Smith Laboratories, 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, delayed release
- Strength
- 250 mg
- Approval
- ANDA ANDA078182
- On the market since
- Nov 1, 2014
- Package NDCs
53808-1027-1- 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?