FdaApplication
ANDA 219129
Identifiers
- fda_app_no: ANDA219129
Properties
| Property | Value |
|---|---|
| applicant_name | NOVITIUM PHARMA LLC |
| application_type | ANDA |
| approval_date | 2025-07-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KETOCONAZOLE | KETOCONAZOLE | 200MG | TABLET;ORAL |
1 product