Drug application
YUTREPIA (TREPROSTINIL SODIUM)
Drugs@FDA NDA 213005 · LIQUIDIA TECH
Key facts
| Drug name | YUTREPIA |
|---|---|
| Active ingredients | TREPROSTINIL SODIUM |
| Application type | NDA |
| Application number | 213005 |
| Company | LIQUIDIA TECH |
| Dosage forms | POWDER, INHALATION |
| Strength | EQ 0.0265MG BASE/INH |
| Marketing status | Prescription |
| Reference listed drug | Yes |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | May 23, 2025 |
At a glance
- 1–9 Submissions
- 1–9 Label versions
- 1–9 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: