kygevvi 2 GM / 2 GM Powder for Oral Solution
- RxCUI
- 2737541
- RxNorm name
- kygevvi 2 GM / 2 GM Powder for Oral Solution
- Display name
- kygevvi 2 GM / 2 GM Powder for Oral Solution
- Full name
- kygevvi 2 GM / 2 GM Powder for Oral Solution
- Term type
- PSN
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:39:05
UNII Substances#
No records found.
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| KYGEVVI | DOXECITINE AND DOXRIBTIMINE | UCB, Inc. | 7d5ce670-9314-4fd7-8b0a-1447910dcf9e | 2025-11-10 | Warnings, Adverse reactions | 2737541 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 7d5ce670-9314-4fd7-8b0a-1447910dcf9e | kygevvi 2 GM / 2 GM Powder for Oral Solution | PSN | 3 | These highlights do not include all the information needed to use KYGEVVI safely and effectively. See full prescribing information for KYGEVVI. KYGEVVI (doxecitine and doxribtimine) powder, for oral solution Initial U.S. Approval: 2025 | 20251110 |
| 7d5ce670-9314-4fd7-8b0a-1447910dcf9e | doxecitine 2000 MG / doxribtimine 2000 MG Powder for Oral Solution [Kygevvi] | SBD | 3 | These highlights do not include all the information needed to use KYGEVVI safely and effectively. See full prescribing information for KYGEVVI. KYGEVVI (doxecitine and doxribtimine) powder, for oral solution Initial U.S. Approval: 2025 | 20251110 |
| 7d5ce670-9314-4fd7-8b0a-1447910dcf9e | Kygevvi (doxecitine 2 GM / doxribtimine 2 GM) Powder for Oral Solution | SY | 3 | These highlights do not include all the information needed to use KYGEVVI safely and effectively. See full prescribing information for KYGEVVI. KYGEVVI (doxecitine and doxribtimine) powder, for oral solution Initial U.S. Approval: 2025 | 20251110 |