NDC 46708-821 – Divalproex sodium
Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Oral
Product NDC46708-821
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA218793
- Marketed since
- December 23, 2024
- 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 |
|---|---|---|
| 46708-821-10 | 100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | Dec 23, 2024 |
| 46708-821-31 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-31) | Dec 23, 2024 |
| 46708-821-91 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-91) | Dec 23, 2024 |
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