NDC 61919-249 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC61919-249
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex sodium
- Labeler
- DirectRx
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- April 6, 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 61919-249-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30) | Apr 6, 2022 |
| 61919-249-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60) | Apr 6, 2022 |
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