NDC 0832-7122 – Divalproex Sodium
Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral
Product NDC0832-7122
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078182
- Marketed since
- March 21, 2014
- Marketing end
- October 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0832-7122-11 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-11) | Mar 21, 2014 |
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
- 50090-7841 Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended 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
- 50090-4861 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