NDC 70518-3055 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC70518-3055
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 23, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 250 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3055-1 | 100 POUCH in 1 BOX (70518-3055-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-2) | Mar 16, 2022 |
| 70518-3055-3 | 100 POUCH in 1 BOX (70518-3055-3) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-4) | Aug 9, 2022 |
| 70518-3055-5 | 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-5) | Jan 4, 2023 |
| 70518-3055-6 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-6) | May 1, 2023 |
| 70518-3055-7 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3055-7) | Jun 30, 2025 |
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