FDA.reportPublic FDA data

prednisolone 10 MG Disintegrating Oral Tablet [Orapred]

RxCUI
668658
RxNorm name
prednisolone 10 MG Disintegrating Oral Tablet [Orapred]
Display name
prednisolone 10 MG Disintegrating Oral Tablet [Orapred]
Full name
prednisolone 10 MG Disintegrating Oral Tablet [Orapred]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:49

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
Orapred ODTPREDNISOLONE SODIUM PHOSPHATEAdvanz Pharma (US) Corp.1e379543-c4cf-4e72-953b-db15b7f0c2a12025-06-03Warnings, Adverse reactionsExact identifier
rxcui: 668658

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
1e379543-c4cf-4e72-953b-db15b7f0c2a1Orapred ODT 10 MG Disintegrating Oral Tablet [PSN] · prednisolone 10 MG Disintegrating Oral Tablet [Orapred] [SBD] · Orapred 10 MG Disintegrating Oral Tablet [SY]312These highlights do not include all the information needed to use ORAPRED ODT ® safely and effectively. See full prescribing information for ORAPRED ODT ® . ORAPRED ODT ® (prednisolone sodium phosphate orally disintegrating tablets) Initial U.S. Approval: 195520250603