NDC 71610-205 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71610-205
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 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71610-205-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-30) | Dec 13, 2018 |
| 71610-205-53 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-53) | Dec 13, 2018 |
| 71610-205-60 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-60) | Dec 13, 2018 |
| 71610-205-70 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-70) | Dec 13, 2018 |
| 71610-205-80 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-80) | Dec 13, 2018 |
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