FDA.reportPublic FDA data

Quillivant XR 300 MG per 60 ML 24 HR Extended Release Suspension

RxCUI
1312589
RxNorm name
Quillivant XR 300 MG per 60 ML 24 HR Extended Release Suspension
Display name
Quillivant XR 300 MG per 60 ML 24 HR Extended Release Suspension
Full name
Quillivant XR 300 MG per 60 ML 24 HR Extended Release Suspension
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:19

RxNav Current And Historical NDCs#

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UNII Substances#

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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
Quillivant XRMETHYLPHENIDATE HYDROCHLORIDENextWave Pharmaceuticals, Incc2dc2109-44a6-4797-b04e-18761dd9d45a2026-03-24Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1312589

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
c2dc2109-44a6-4797-b04e-18761dd9d45aQuillivant XR 25 MG in 5 mL 24HR Extended Release Oral Suspension [PSN] · 24 HR methylphenidate hydrochloride 5 MG/ML Extended Release Suspension [Quillivant] [SBD] · 24 HR Quillivant 5 MG/ML Extended Release Suspension [SY] · Quillivant XR 25 MG per 5 ML 24 HR Extended Release Suspension [SY] · Quillivant XR 300 MG per 60 ML 24 HR Extended Release Suspension [SY] · Quillivant XR 600 MG per 120 ML 24 HR Extended Release Suspension [SY] · Quillivant XR 750 MG per 150 ML 24 HR Extended Release Suspension [SY] · Quillivant XR 900 MG per 180 ML 24 HR Extended Release Suspension [SY]820These highlights do not include all the information needed to use QUILLIVANT XR ® safely and effectively. See full prescribing information for QUILLIVANT XR ® . QUILLIVANT XR ® (methylphenidate hydrochloride) for extended-release oral suspension, CII Initial U.S. Approval: 195520260320