Divalproex Sodium 60687-0915-01
- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 29, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA214643
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 500 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Selected Package
60687-0915-01Selected100 BLISTER PACK in 1 CARTON (60687-915-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-11)
Other packages for this product(1)
80 BLISTER PACK in 1 CARTON (60687-915-02) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-93)