NDC 54868-6072
Divalproex Sodium 500 mg tablet, delayed release
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0093-7441, made by Teva 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. 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Valproic Acid: every company that makes it
- Form
- tablet, delayed release
- Strength
- 500 mg
- Approval
- ANDA ANDA076941
- On the market since
- Oct 15, 2009
- Package NDCs
54868-6072-054868-6072-154868-6072-254868-6072-3- Official label
- DailyMed (National Library of Medicine), updated Jan 4, 2010
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