NDC 70518-2357 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC70518-2357
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090554
- Marketed since
- October 10, 2019
- 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 |
|---|---|---|
| 70518-2357-0 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-0) | Oct 10, 2019 |
| 70518-2357-1 | 100 POUCH in 1 BOX (70518-2357-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2357-2) | Mar 16, 2021 |
| 70518-2357-5 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-5) | Aug 9, 2022 |
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