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#

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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.

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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#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
1e379543-c4cf-4e72-953b-db15b7f0c2a1prednisolone 10 MG Disintegrating Oral Tablet [Orapred]SBD12These 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
1e379543-c4cf-4e72-953b-db15b7f0c2a1Orapred ODT 10 MG Disintegrating Oral TabletPSN12These 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
1e379543-c4cf-4e72-953b-db15b7f0c2a1Orapred 10 MG Disintegrating Oral TabletSY12These 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