FdaApplication
ANDA 205904
Identifiers
- fda_app_no: ANDA205904
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN INC |
| application_type | ANDA |
| approval_date | 2024-01-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DRONEDARONE HYDROCHLORIDE | DRONEDARONE HYDROCHLORIDE | EQ 400MG BASE | TABLET;ORAL |
1 product