NDC 0904-6363 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0904-6363
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090161
- Marketed since
- August 11, 2013
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 0904-6363-45 | 80 BLISTER PACK in 1 CARTON (0904-6363-45) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Aug 11, 2013 |
| 0904-6363-61 | 100 BLISTER PACK in 1 CARTON (0904-6363-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Aug 11, 2013 |
Recalls mentioning this NDC
- D-1583-2019 Aug 7, 2019 · Class II
cGMP deviations: Product was exposed above 50% relative humidity levels during packaging operations.
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