NDC 68084-782 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC68084-782
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090554
- Marketed since
- January 26, 2016
- 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 (0)
| Package NDC | Description | Since |
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