NDC 60687-879 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC60687-879
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- February 6, 2025
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 60687-879-61 | 90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11) | Feb 6, 2025 |
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