mesalamine 66.7 MG/ML Enema [Rowasa]

RxCUI
206798
RxNorm name
mesalamine 66.7 MG/ML Enema [Rowasa]
Display name
mesalamine 66.7 MG/ML Enema [Rowasa]
Full name
mesalamine 66.7 MG/ML Enema [Rowasa]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:25

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
RowasaMESALAMINEViatris Specialty LLCe505ab99-1943-4216-a178-4d5dbe64e3b22026-08-03Warnings, Adverse reactionsExact identifier
rxcui: 206798

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
e505ab99-1943-4216-a178-4d5dbe64e3b2sfRowasa 4 GM in 60 mL Enema [PSN] · mesalamine 66.7 MG/ML Enema [Rowasa] [SBD] · Rowasa 4 GM per 60 ML Enema [SY] · Rowasa 66.7 MG/ML Enema [SY] · sfRowasa 4 GM per 60 ML Enema [SY]517These highlights do not include all the information needed to use ROWASA safely and effectively. See full prescribing information for ROWASA . ROWASA (mesalamine) rectal suspension Initial U.S. Approval: 198720240715
aa273fdc-f7c4-4901-8f71-59ae03b8cdb1sfRowasa 4 GM in 60 mL Enema [PSN] · mesalamine 66.7 MG/ML Enema [Rowasa] [SBD] · Rowasa 4 GM per 60 ML Enema [SY] · Rowasa 66.7 MG/ML Enema [SY] · sfRowasa 4 GM per 60 ML Enema [SY]512These highlights do not include all the information needed to use sfROWASA safely and effectively. See full prescribing information for sfROWASA. sfROWASA® (mesalamine) rectal suspension sulfite-free formulation Initial U.S. Approval: 198720240724