NDC 68001-472 – Divalproex Sodium
Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral
Product NDC68001-472
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- January 20, 2021
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 68001-472-00 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00) | Jan 20, 2021 |
| 68001-472-03 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03) | Jan 20, 2021 |
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