FdaApplication
ANDA 213708
Identifiers
- fda_app_no: ANDA213708
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2024-11-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EPINEPHRINE | EPINEPHRINE | 1MG/ML (1MG/ML) | SOLUTION;INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS |
1 product