FdaApplication
ANDA 217665
Identifiers
- fda_app_no: ANDA217665
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2023-05-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METRONIDAZOLE IN PLASTIC CONTAINER | METRONIDAZOLE | 500MG/100ML | INJECTABLE;INJECTION |
1 product