VENXXIVA 100 MG Delayed Release Oral Tablet
- RxCUI
- 2702682
- RxNorm name
- VENXXIVA 100 MG Delayed Release Oral Tablet
- Display name
- VENXXIVA 100 MG Delayed Release Oral Tablet
- Full name
- VENXXIVA 100 MG Delayed Release Oral Tablet
- Term type
- PSN
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:38:45
UNII Substances#
No records found.
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| VENXXIVA | TIOPRONIN | Cycle Pharmaceuticals Ltd. | 02e24443-04c6-4b98-a395-49aec4a468de | 2025-12-22 | Warnings, Adverse reactions | 2702682 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 02e24443-04c6-4b98-a395-49aec4a468de | VENXXIVA 100 MG Delayed Release Oral Tablet | PSN | 2 | These highlights do not include all the information needed to use VENXXIVA TM safely and effectively. See full prescribing information for VENXXIVA. VENXXIVA (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251222 |
| 02e24443-04c6-4b98-a395-49aec4a468de | tiopronin 100 MG Delayed Release Oral Tablet [Venxxiva] | SBD | 2 | These highlights do not include all the information needed to use VENXXIVA TM safely and effectively. See full prescribing information for VENXXIVA. VENXXIVA (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251222 |
| 02e24443-04c6-4b98-a395-49aec4a468de | Venxxiva 100 MG Delayed Release Oral Tablet | SY | 2 | These highlights do not include all the information needed to use VENXXIVA TM safely and effectively. See full prescribing information for VENXXIVA. VENXXIVA (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251222 |