FdaApplication
NDA 019680
Identifiers
- fda_app_no: NDA019680
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1989-09-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEPAKOTE | DIVALPROEX SODIUM | EQ 125MG VALPROIC ACID | CAPSULE, DELAYED REL PELLETS;ORAL |
1 product