NDC 67296-1635
Divalproex Sodium 250 mg tablet, film coated, extended release
On the label: RedPharm Drug. Inc.. It's repackaged from NDC 0115-6911, made by Amneal Pharmaceuticals of New York LLC (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 and relabels 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 RedPharm Drug. Inc. names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 250 mg
- Approval
- ANDA ANDA078791
- On the market since
- Jan 1, 2019
- Package NDCs
67296-1635-1- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2021
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