FDA.reportPublic FDA data

DPH 25 MG/ML Oral Suspension [Dilantin]

RxCUI
1313884
RxNorm name
DPH 25 MG/ML Oral Suspension [Dilantin]
Display name
DPH 25 MG/ML Oral Suspension [Dilantin]
Full name
DPH 25 MG/ML Oral Suspension [Dilantin]
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:27

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dilantin-125PHENYTOINViatris Specialty LLCf339f9e4-b289-4efe-82b9-46c57d1dc2772023-02-02Warnings, Adverse reactionsExact identifier
rxcui: 1313884

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
f339f9e4-b289-4efe-82b9-46c57d1dc277Dilantin-125, 125 MG in 5 mL Oral Suspension [PSN] · phenytoin 25 MG/ML Oral Suspension [Dilantin] [SBD] · Dilantin 125 MG per 5 ML Oral Suspension [SY] · Dilantin 25 MG/ML Oral Suspension [SY] · Dilantin-125 Oral Suspension [SY] · DPH 25 MG/ML Oral Suspension [Dilantin] [SY]61These highlights do not include all the information needed to use DILANTIN-125 ® safely and effectively. See full prescribing information for DILANTIN-125 ® . DILANTIN-125® (phenytoin) oral suspension Initial U.S. Approval: 195320230202