NDC 29300-139 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC29300-139
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- October 1, 2011
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 29300-139-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01) | Oct 1, 2011 |
| 29300-139-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05) | Oct 1, 2011 |
| 29300-139-10 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10) | Oct 1, 2011 |
Recalls mentioning this NDC
- D-0228-2018 Jan 24, 2018 · Class II
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
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