Thiola 300 MG Delayed Release Oral Tablet
- RxCUI
- 2178081
- RxNorm name
- Thiola 300 MG Delayed Release Oral Tablet
- Display name
- Thiola 300 MG Delayed Release Oral Tablet
- Full name
- Thiola 300 MG Delayed Release Oral Tablet
- Term type
- SY
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:38:50
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 |
|---|---|---|---|---|---|---|
| Thiola EC | TIOPRONIN | Mission Pharmacal Company | 20298a52-a194-a161-8632-d84b6f26e23c | 2025-10-07 | Warnings, Adverse reactions | 2178081 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 20298a52-a194-a161-8632-d84b6f26e23c | Thiola 300 MG Delayed Release Oral Tablet | SY | 6 | These highlights do not include all the information needed to use THIOLA EC ® safely and effectively. See full prescribing information for THIOLA EC. THIOLA EC (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251007 |
| 20298a52-a194-a161-8632-d84b6f26e23c | THIOLA EC 300 MG Delayed Release Oral Tablet | PSN | 6 | These highlights do not include all the information needed to use THIOLA EC ® safely and effectively. See full prescribing information for THIOLA EC. THIOLA EC (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251007 |
| 20298a52-a194-a161-8632-d84b6f26e23c | tiopronin 300 MG Delayed Release Oral Tablet [Thiola] | SBD | 6 | These highlights do not include all the information needed to use THIOLA EC ® safely and effectively. See full prescribing information for THIOLA EC. THIOLA EC (tiopronin) delayed-release tablets, for oral use Initial U.S. Approval: 1988 | 20251007 |