NDC 71335-1883 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-1883
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209286
- Marketed since
- September 18, 2020
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1883-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-1) | Jul 18, 2024 |
| 71335-1883-2 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-2) | Jun 21, 2021 |
| 71335-1883-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-3) | Aug 18, 2022 |
| 71335-1883-4 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1883-4) | Aug 18, 2022 |
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