maraviroc 20 MG per 1 ML Oral Solution

RxCUI
1857921
RxNorm name
maraviroc 20 MG per 1 ML Oral Solution
Display name
maraviroc 20 MG per 1 ML Oral Solution
Full name
maraviroc 20 MG per 1 ML Oral Solution
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:56

RxNav Current And Historical NDCs#

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UNII Substances#

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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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SELZENTRYMARAVIROCViiV Healthcare Company46f30ac5-c96b-429e-976d-8c5ee1c0761b2022-09-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1857921

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
46f30ac5-c96b-429e-976d-8c5ee1c0761bmaraviroc 20 MG per 1 ML Oral SolutionSY25These highlights do not include all the information needed to use SELZENTRY safely and effectively. See full prescribing information for SELZENTRY. SELZENTRY (maraviroc) tablets, for oral use SELZENTRY (maraviroc) oral solution Initial U.S. Approval: 200720220926
46f30ac5-c96b-429e-976d-8c5ee1c0761bmaraviroc 20 MG/ML Oral SolutionSCD25These highlights do not include all the information needed to use SELZENTRY safely and effectively. See full prescribing information for SELZENTRY. SELZENTRY (maraviroc) tablets, for oral use SELZENTRY (maraviroc) oral solution Initial U.S. Approval: 200720220926
46f30ac5-c96b-429e-976d-8c5ee1c0761bmaraviroc 20 MG in 1 mL Oral SolutionPSN25These highlights do not include all the information needed to use SELZENTRY safely and effectively. See full prescribing information for SELZENTRY. SELZENTRY (maraviroc) tablets, for oral use SELZENTRY (maraviroc) oral solution Initial U.S. Approval: 200720220926