Tembexa 4 Tablet Pack

RxCUI
2599541
RxNorm name
Tembexa 4 Tablet Pack
Display name
Tembexa 4 Tablet Pack
Full name
Tembexa 4 Tablet Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:53

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
TembexaBRINCIDOFOVIREmergent BioDefense Operations Lansing LLC209aa94b-c613-4880-ad89-41be83d12c0a2025-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2599541

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
31d6fa29-791e-4988-8758-e7e4d5b6a352{4 (brincidofovir 100 MG Oral Tablet [Tembexa]) } Pack [Tembexa 4 Tablet Pack] [BPCK] · TEMBEXA 4 Tablet Pack [PSN] · Tembexa 4 Tablet Pack [SY]34These highlights do not include all the information needed to use TEMBEXA ® safely and effectively. See full prescribing information for TEMBEXA. TEMBEXA (brincidofovir) tablets, for oral use TEMBEXA (brincidofovir) oral suspension Initial U.S. Approval: 199620220418
209aa94b-c613-4880-ad89-41be83d12c0a{4 (brincidofovir 100 MG Oral Tablet [Tembexa]) } Pack [Tembexa 4 Tablet Pack] [BPCK] · TEMBEXA 4 Tablet Pack [PSN] · Tembexa 4 Tablet Pack [SY]32These highlights do not include all the information needed to use TEMBEXA ® safely and effectively. See full prescribing information for TEMBEXA . TEMBEXA (brincidofovir) tablets, for oral use TEMBEXA (brincidofovir) oral suspension Initial U.S. Approval: 199620250701