NDC 68001-106 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68001-106
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078239
- Marketed since
- October 8, 2013
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 68001-106-00 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00) | Oct 8, 2013 |
| 68001-106-03 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-03) | Oct 8, 2013 |
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