NDC 68071-3553 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC68071-3553
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 |
|---|---|---|
| 68071-3553-6 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6) | Dec 7, 2023 |
Other Divalproex Sodium products
- 50090-7635 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-1123 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-2007 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-4861 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-7121 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-7763 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 68084-776 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · American Health Packaging
- 60687-868 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · American Health Packaging
- 68084-782 Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · American Health Packaging
- 60687-879 Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · American Health Packaging
- 60687-857 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · American Health Packaging
- 71610-031 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Aphena Pharma Solutions - Tennessee, LLC