Drug application
ARTESUNATE (ARTESUNATE)
Drugs@FDA NDA 213170 · LA JOLLA PHARMA
Key facts
| Drug name | ARTESUNATE |
|---|---|
| Active ingredients | ARTESUNATE |
| Application type | NDA |
| Application number | 213170 |
| Company | LA JOLLA PHARMA |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | UNKNOWN |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | May 29, 2020 |
At a glance
- 1–9 Submissions
- None Label versions
- None Products
- None Therapeutic equivalents
- Yes FDA letters on file
- No FDA reviews on file
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: