Divalproex Sodium Extended-Release Tablets Recalled for Failed Dissolution Specifications
Amneal Pharmaceuticals is recalling 4,309 bottles of Divalproex Sodium Extended-Release Tablets (250 mg) due to failed dissolution specifications. The tablets may not dissolve properly, potentially affecting medication effectiveness.
- Product
- DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
- Category
- Drug
- Distribution
- Distributed nationwide