FdaApplication
ANDA 076539
Identifiers
- fda_app_no: ANDA076539
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2003-06-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VALPROATE SODIUM | VALPROATE SODIUM | EQ 100MG BASE/ML | INJECTABLE;INJECTION |
1 product