NDC 50090-2007 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC50090-2007
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- October 1, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 250 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-2007-0 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-0) | Sep 18, 2015 |
| 50090-2007-1 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-1) | Aug 2, 2017 |
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