NDC 65841-639 – Divalproex sodium
Divalproex Sodium 125 mg/1 · Capsule, Coated Pellets · Oral
Product NDC65841-639
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA078919
- Marketed since
- January 27, 2009
- Listing expires
- December 31, 2026
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 65841-639-01 | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-01) | Jan 27, 2009 |
| 65841-639-10 | 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (65841-639-10) | Jan 27, 2009 |
| 65841-639-30 | 10 BLISTER PACK in 1 CARTON (65841-639-30) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK | Jan 27, 2009 |
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