NDC 70518-1781 – Divalproex sodium
Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70518-1781
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202419
- Marketed since
- January 7, 2019
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1781-1 | 100 POUCH in 1 BOX (70518-1781-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1781-2) | Aug 3, 2020 |
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