NDC 71610-289 – Divalproex sodium
Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71610-289
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202419
- Marketed since
- June 2, 2014
- Listing expires
- December 31, 2026
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 71610-289-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-30) | Jun 5, 2019 |
| 71610-289-60 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-60) | Jun 5, 2019 |
| 71610-289-75 | 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-75) | Jun 5, 2019 |
| 71610-289-80 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-80) | Sep 3, 2024 |
| 71610-289-92 | 270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-92) | Sep 3, 2024 |
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