Depakote ER 250 mg/1
Divalproex Sodium · TABLET, EXTENDED RELEASE · AbbVie Inc.
No Recall History
Plain English
Depakote ER is a tablet, extended release containing divalproex sodium at 250 mg/1, taken oral. Manufactured by AbbVie Inc..
Key Facts
- Brand Name
- Depakote ER
- Generic Name
- Divalproex Sodium
- NDC Code (Product)
0074-7401- Manufacturer
- AbbVie Inc.
- Strength
- 250 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA021168
- Marketing Start
- 08/04/2000
Recall History
No Recall HistoryFrequently Asked Questions
What is Depakote ER used for?
Depakote ER contains Divalproex Sodium. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is Depakote ER a controlled substance?
Depakote ER is not classified as a controlled substance by the DEA.
What is the generic name for Depakote ER?
The generic name for Depakote ER is Divalproex Sodium. There are 12 other brand versions of Divalproex Sodium.
What is the NDC code for Depakote ER 250 mg/1?
The NDC (National Drug Code) for Depakote ER 250 mg/1 is 0074-7401, listed by AbbVie Inc..
Other Divalproex Brands
See all →- Divalproex Sodium250 mg/172789-353
- Divalproex Sodium250 mg/10615-8327
- Divalproex sodium250 mg/10615-8376
- Divalproex sodium125 mg/127241-115
- Divalproex Sodium125 mg/129300-138
- Divalproex Sodium100 [hp_C]/137662-2865
- Divalproex Sodium200 [hp_C]/137662-2866
- Divalproex sodium500 mg/150090-6074
- Divalproex Sodium125 mg/150090-7635
- divalproex sodium500 mg/150090-7841
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)