FDA.reportPublic FDA data

Humalog Mix 75/25 300 UNT per 3 ML Pen

RxCUI
847254
RxNorm name
Humalog Mix 75/25 300 UNT per 3 ML Pen
Display name
Humalog Mix 75/25 300 UNT per 3 ML Pen
Full name
Humalog Mix 75/25 300 UNT per 3 ML Pen
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:20

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
021017Humalog Mix 75/25insulin lispro protamine and insulin lispro351(a)Rx2026-07-01

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
Humalog Mix75/25 KwikPenINSULIN LISPROEli Lilly and Companyc73da51a-1899-45ad-b6cf-9c52c36a25dd2024-08-06Warnings, Adverse reactionsExact identifier
rxcui: 847254

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
c73da51a-1899-45ad-b6cf-9c52c36a25ddHumaLOG Mix 75/25 UNT in 3 ML Pen Injector [PSN] · 3 ML insulin lispro 25 UNT/ML / insulin lispro protamine, human 75 UNT/ML Pen Injector [Humalog Mix] [SBD] · Humalog Mix 75/25 300 UNT per 3 ML KwikPen [SY] · Humalog Mix 75/25 300 UNT per 3 ML Pen [SY]453These highlights do not include all the information needed to use HUMALOG MIX75/25 safely and effectively. See full prescribing information for HUMALOG MIX75/25. HUMALOG MIX75/25 (insulin lispro protamine and insulin lispro) injectable suspension, for subcutaneous use Initial U.S. Approval: 199920240806