NDC 65162-757 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC65162-757
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203730
- Marketed since
- June 1, 2015
- Listing expires
- December 31, 2027
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 65162-757-10 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-10) | Jun 1, 2015 |
| 65162-757-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-50) | Jun 1, 2015 |
Recalls mentioning this NDC
- D-0426-2024 Apr 3, 2024 · Class II
Failed dissolution specifications - D-1362-2022 Aug 31, 2022 · Class II
Failed dissolution specifications.
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