NDC 70518-2674 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC70518-2674
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078597
- Marketed since
- April 6, 2020
- 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 |
|---|---|---|
| 70518-2674-0 | 100 POUCH in 1 BOX (70518-2674-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2674-1) | Apr 6, 2020 |
| 70518-2674-2 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2) | Apr 30, 2021 |
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