FdaApplication
ANDA 206018
Identifiers
- fda_app_no: ANDA206018
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LLC |
| application_type | ANDA |
| approval_date | 2016-12-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MELPHALAN HYDROCHLORIDE | MELPHALAN HYDROCHLORIDE | EQ 50MG BASE/VIAL | INJECTABLE;INJECTION |
1 product