3 ML insulin, regular, human 100 UNT/ML Pen Injector [Novolin R]

RxCUI
2206092
RxNorm name
3 ML insulin, regular, human 100 UNT/ML Pen Injector [Novolin R]
Display name
3 ML insulin, regular, human 100 UNT/ML Pen Injector [Novolin R]
Full name
3 ML insulin, regular, human 100 UNT/ML Pen Injector [Novolin R]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:16

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
019938Novolin Rinsulin human351(a)OTC2026-07-01

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
Novolin RHUMAN INSULINNovo Nordiskaee7f1f3-612c-4027-8ce9-4fd1f41eed712022-11-23Warnings, Adverse reactionsExact identifier
rxcui: 2206092

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
aee7f1f3-612c-4027-8ce9-4fd1f41eed71NovoLIN R 100 UNT/mL in 3 mL Pen Injector [PSN] · 3 ML insulin, regular, human 100 UNT/ML Pen Injector [Novolin R] [SBD] · 3 ML Novolin R 100 UNT/ML Pen Injector [SY] · Novolin R 100 UNT/ML per 3 ML Pen Injector [SY] · Relion Novolin R 100 UNT/ML per 3 ML Pen Injector [SY]519These highlights do not include all the information needed to use NOVOLIN R safely and effectively. See full prescribing information for NOVOLIN R. NOVOLIN ® R (insulin human) injection, for subcutaneous or intravenous use Initial U.S. Approval: 199120221123