NDC 71610-032 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC71610-032
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078182
- Marketed since
- March 21, 2014
- 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 |
|---|---|---|
| 71610-032-53 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53) | Jan 19, 2018 |
| 71610-032-60 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60) | Jan 19, 2018 |
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