FdaApplication
ANDA 074419
Identifiers
- fda_app_no: ANDA074419
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 1995-03-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZATHIOPRINE SODIUM | AZATHIOPRINE SODIUM | EQ 100MG BASE/VIAL | INJECTABLE;INJECTION |
1 product