Divalproex Sodium 70518-3683
Product NDC
70518-3683- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 17, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA090554
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 125 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(3)
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-0)
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-1)
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3683-2)