FdaApplication
ANDA 078700
Identifiers
- fda_app_no: ANDA078700
Properties
| Property | Value |
|---|---|
| applicant_name | COSETTE PHARMACEUTICALS NC LABORATORIES LLC |
| application_type | ANDA |
| approval_date | 2009-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIVALPROEX SODIUM | DIVALPROEX SODIUM | EQ 500MG VALPROIC ACID | TABLET, EXTENDED RELEASE;ORAL |
1 product