FdaApplication
ANDA 208120
Identifiers
- fda_app_no: ANDA208120
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMOBEDIENT CONSULTING LLC |
| application_type | ANDA |
| approval_date | 2021-12-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VALPROATE SODIUM | VALPROATE SODIUM | EQ 100MG BASE/ML | INJECTABLE;INJECTION |
1 product