FdaApplication
NDA 020207
Identifiers
- fda_app_no: NDA020207
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | NDA |
| approval_date | 1992-11-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALKERAN | MELPHALAN HYDROCHLORIDE | EQ 50MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
1 product