Baraclude 0.5 MG Oral Tablet

RxCUI
578457
RxNorm name
Baraclude 0.5 MG Oral Tablet
Display name
Baraclude 0.5 MG Oral Tablet
Full name
Baraclude 0.5 MG Oral Tablet
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:46

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
BARACLUDEENTECAVIRE.R. Squibb & Sons, L.L.C.046e61c9-9298-4b2e-b76e-b26b81fecd202019-11-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 578457

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
046e61c9-9298-4b2e-b76e-b26b81fecd20Baraclude 0.5 MG Oral TabletPSN42These highlights do not include all the information needed to use BARACLUDE safely and effectively. See full prescribing information for BARACLUDE. BARACLUDE ® (entecavir) tablets, for oral use BARACLUDE ® (entecavir) oral solution Initial U.S. Approval: 200520191106
046e61c9-9298-4b2e-b76e-b26b81fecd20Baraclude 0.5 MG Oral TabletSY42These highlights do not include all the information needed to use BARACLUDE safely and effectively. See full prescribing information for BARACLUDE. BARACLUDE ® (entecavir) tablets, for oral use BARACLUDE ® (entecavir) oral solution Initial U.S. Approval: 200520191106
046e61c9-9298-4b2e-b76e-b26b81fecd20entecavir 0.5 MG Oral Tablet [Baraclude]SBD42These highlights do not include all the information needed to use BARACLUDE safely and effectively. See full prescribing information for BARACLUDE. BARACLUDE ® (entecavir) tablets, for oral use BARACLUDE ® (entecavir) oral solution Initial U.S. Approval: 200520191106