NDC 17856-0797 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC17856-0797
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078597
- Marketed since
- July 29, 2008
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 17856-0797-1 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-0797-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH | Nov 2, 2018 |
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