FDA.reportPublic FDA data

Nithiodote Kit

RxCUI
1086836
RxNorm name
Nithiodote Kit
Display name
Nithiodote Kit
Full name
Nithiodote Kit
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:30

RxNav Current And Historical NDCs#

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

No records found.

UNII Substances#

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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
NITHIODOTESODIUM NITRITE AND SODIUM THIOSULFATEHope Pharmaceuticalsff4941b3-9901-4aab-adcf-c5327bede34e2025-10-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1086836

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
ff4941b3-9901-4aab-adcf-c5327bede34e{1 (10 ML sodium nitrite 30 MG/ML Injection) / 1 (50 ML sodium thiosulfate 250 MG/ML Injection) } Pack [Nithiodote] [BPCK] · Nithiodote Pack [PSN] · Nithiodote Kit [SY]310These highlights do not include all the information needed to use the NITHIODOTE safely and effectively. See full prescribing information for NITHIODOTE. NITHIODOTE (sodium nitrite injection and sodium thiosulfate injection for intravenous infusion). Initial U.S. Approval: 199220251006