FdaApplication
ANDA 218208
Identifiers
- fda_app_no: ANDA218208
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2025-12-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EPINEPHRINE | EPINEPHRINE | EQ 1MG BASE/ML (EQ 1MG BASE/ML) | SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
1 product