FdaApplication
ANDA 212001
Identifiers
- fda_app_no: ANDA212001
Properties
| Property | Value |
|---|---|
| applicant_name | CUSTOPHARM INC |
| application_type | ANDA |
| approval_date | 2019-06-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GANCICLOVIR SODIUM | GANCICLOVIR SODIUM | EQ 500MG BASE/VIAL | INJECTABLE;INJECTION |
1 product