NDC 62756-797 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC62756-797
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078597
- Marketed since
- July 29, 2008
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 62756-797-08 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08) | Jul 29, 2008 |
| 62756-797-13 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13) | Jul 29, 2008 |
| 62756-797-18 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18) | Jul 29, 2008 |
| 62756-797-83 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83) | Jul 29, 2008 |
| 62756-797-88 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88) | Jul 29, 2008 |
Recalls mentioning this NDC
- D-1291-2022 Aug 3, 2022 · Class II
Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.
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