FdaApplication
ANDA 204817
Identifiers
- fda_app_no: ANDA204817
Properties
| Property | Value |
|---|---|
| applicant_name | ALMAJECT INC |
| application_type | ANDA |
| approval_date | 2019-05-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MELPHALAN HYDROCHLORIDE | MELPHALAN HYDROCHLORIDE | EQ 50MG BASE/VIAL | INJECTABLE;INJECTION |
1 product