Drug application
KYGEVVI (DOXECITINE, DOXRIBTIMINE)
Drugs@FDA NDA 219792 · UCB INC
Key facts
| Drug name | KYGEVVI |
|---|---|
| Active ingredients | DOXECITINE, DOXRIBTIMINE |
| Application type | NDA |
| Application number | 219792 |
| Company | UCB INC |
| Dosage forms | FOR SOLUTION, ORAL |
| Strength | 2GM/PACKET;2GM/PACKET |
| Marketing status | Prescription |
| Reference listed drug | Yes |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Nov 3, 2025 |
At a glance
- 1–9 Submissions
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- Yes 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: