NDC 55111-534 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC55111-534
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Dr. Reddy's Laboratories Ltd
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090070
- Marketed since
- August 11, 2013
- Listing expires
- December 31, 2027
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-534-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-01) | Aug 11, 2013 |
| 55111-534-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-05) | Aug 11, 2013 |
| 55111-534-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-30) | Aug 11, 2013 |
| 55111-534-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-534-60) | Aug 11, 2013 |
Recalls mentioning this NDC
- D-1136-2015 Jun 24, 2015 · Class II
Failed Dissolution Specifications; exceeded specification at the 9 hour time point
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