NDC 69452-435 – divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC69452-435
Product details
- Brand name
- divalproex sodium
- Generic name
- divalproex sodium
- Labeler
- Bionpharma Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078853
- Marketed since
- June 26, 2024
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 69452-435-13 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-13) | Jun 26, 2024 |
| 69452-435-20 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20) | Jun 26, 2024 |
| 69452-435-30 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30) | Jun 26, 2024 |
Recalls mentioning this NDC
- D-0742-2026 Jul 29, 2026 · Class II
Presence of Foreign Tablets/Capsules
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