NDC 71335-2158 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC71335-2158
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090554
- Marketed since
- October 24, 2014
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2158-1 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1) | Aug 11, 2022 |
| 71335-2158-2 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2) | Mar 2, 2023 |
| 71335-2158-3 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3) | Aug 11, 2022 |
| 71335-2158-4 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4) | Sep 6, 2024 |
| 71335-2158-5 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5) | Sep 20, 2022 |
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