NDC 68180-265 – Divalproex Sodium
Divalproex Sodium 125 mg/1 · Tablet, Delayed Release · Oral
Product NDC68180-265
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078790
- Marketed since
- July 29, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (0)
| Package NDC | Description | Since |
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