FdaApplication
NDA 019794
Identifiers
- fda_app_no: NDA019794
Properties
| Property | Value |
|---|---|
| applicant_name | ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV |
| application_type | NDA |
| approval_date | 1990-07-11 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEPAKOTE CP | DIVALPROEX SODIUM | EQ 500MG BASE | TABLET, DELAYED RELEASE;ORAL |
| DEPAKOTE CP | DIVALPROEX SODIUM | EQ 250MG BASE | TABLET, DELAYED RELEASE;ORAL |
2 products