FDA.reportPublic FDA data

tiopronin 300 MG Delayed Release Oral Tablet [Venxxiva]

RxCUI
2702684
RxNorm name
tiopronin 300 MG Delayed Release Oral Tablet [Venxxiva]
Display name
tiopronin 300 MG Delayed Release Oral Tablet [Venxxiva]
Full name
tiopronin 300 MG Delayed Release Oral Tablet [Venxxiva]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:45

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VENXXIVATIOPRONINCycle Pharmaceuticals Ltd.02e24443-04c6-4b98-a395-49aec4a468de2025-12-22Warnings, Adverse reactionsExact identifier
rxcui: 2702684

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
02e24443-04c6-4b98-a395-49aec4a468deVENXXIVA 300 MG Delayed Release Oral Tablet [PSN] · tiopronin 300 MG Delayed Release Oral Tablet [Venxxiva] [SBD] · Venxxiva 300 MG Delayed Release Oral Tablet [SY]32These 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: 198820251222