NDC 0832-7123 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC0832-7123
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078182
- Marketed since
- March 21, 2014
- Marketing end
- October 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 0832-7123-01 | 100 BLISTER PACK in 1 CARTON (0832-7123-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7123-89) | Apr 1, 2016 |
| 0832-7123-11 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7123-11) | Mar 21, 2014 |
| 0832-7123-15 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7123-15) | Mar 21, 2014 |
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