NDC 67046-122
Divalproex Sodium 500 mg tablet, film coated, extended release
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. 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.
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
- Aug 18, 2010
- Package NDCs
67046-122-30- Official label
- DailyMed (National Library of Medicine), updated Aug 18, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?