FdaApplication
ANDA 218745
Identifiers
- fda_app_no: ANDA218745
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX CORP |
| application_type | ANDA |
| approval_date | 2024-08-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CUPRIC SULFATE | CUPRIC SULFATE | EQ 0.4MG COPPER/ML | INJECTABLE;INJECTION |
1 product