Divalproex Sodium 68180-0261-02
- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 18, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA209286
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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
68180-0261-02Selected500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02)
Other packages for this product(1)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-01)