NDC 67046-2021 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Extended Release · Oral
Product NDC67046-2021
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Coupler LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090161
- Marketed since
- June 1, 2026
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 67046-2021-3 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-2021-3) | Jun 1, 2026 |
Other Divalproex Sodium products
- 50090-7635 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-2007 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-4737 Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · A-S Medication Solutions
- 50090-7763 Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-7841 Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · A-S Medication Solutions
- 50090-4861 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
- 50090-7121 Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · A-S Medication Solutions
- 50090-6074 Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · A-S Medication Solutions
- 27241-115 Divalproex Sodium 125 mg/1 · Capsule, Coated Pellets · Ajanta Pharma USA Inc.
- 62332-821 Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Alembic Pharmaceuticals Inc.
- 46708-821 Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Alembic Pharmaceuticals Limited