FdaApplication
NDA 020782
Identifiers
- fda_app_no: NDA020782
Properties
| Property | Value |
|---|---|
| applicant_name | ABBOTT |
| application_type | NDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEPAKOTE ER | DIVALPROEX SODIUM | 250MG | Tablet, Extended Release;Oral |
| DEPAKOTE ER | DIVALPROEX SODIUM | 500MG | Tablet, Extended Release;Oral |
2 products