NDC 0615-8377 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC0615-8377
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209286
- Marketed since
- September 18, 2020
- Marketing end
- October 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 |
|---|---|---|
| 0615-8377-39 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8377-39) | Feb 3, 2021 |
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