NDC 70518-3683 – Divalproex Sodium
Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral
Product NDC70518-3683
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
- March 17, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3683-0 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-0) | Mar 17, 2023 |
| 70518-3683-1 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-1) | Sep 13, 2023 |
| 70518-3683-2 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3683-2) | Jul 1, 2025 |
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