FdaApplication
ANDA 211549
Identifiers
- fda_app_no: ANDA211549
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2022-02-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZACITIDINE | AZACITIDINE | 100MG/VIAL | POWDER;INTRAVENOUS, SUBCUTANEOUS |
1 product