NDC 70518-3477 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC70518-3477
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209286
- Marketed since
- August 16, 2022
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3477-0 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3477-0) | Aug 16, 2022 |
| 70518-3477-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1) | Oct 14, 2022 |
| 70518-3477-3 | 100 POUCH in 1 BOX (70518-3477-3) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-4) | May 17, 2023 |
| 70518-3477-5 | 100 POUCH in 1 BOX (70518-3477-5) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6) | Aug 23, 2023 |
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