Drug application
EPINEPHRINE (EPINEPHRINE)
Drugs@FDA ANDA 213708 · FRESENIUS KABI USA
Key facts
| Drug name | EPINEPHRINE |
|---|---|
| Active ingredients | EPINEPHRINE |
| Application type | ANDA |
| Application number | 213708 |
| Company | FRESENIUS KABI USA |
| Dosage forms | SOLUTION, INTRAVENOUS, INTRAOCULAR, INTRAMUSCULAR, SUBCUTANEOUS |
| Strength | 1MG/ML (1MG/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Nov 20, 2024 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.