NDC 87441-028 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC87441-028
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Unit Dose Solutions, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- June 17, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 87441-028-01 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (87441-028-01) | Jun 17, 2026 |
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