FdaApplication
NDA 018723
Identifiers
- fda_app_no: NDA018723
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1983-03-10 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEPAKOTE | DIVALPROEX SODIUM | EQ 500MG VALPROIC ACID | TABLET, DELAYED RELEASE;ORAL |
| DEPAKOTE | DIVALPROEX SODIUM | EQ 250MG VALPROIC ACID | TABLET, DELAYED RELEASE;ORAL |
| DEPAKOTE | DIVALPROEX SODIUM | EQ 125MG VALPROIC ACID | TABLET, DELAYED RELEASE;ORAL |
3 products