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Humalog®
- Full Prescribing Information
Humalog® U-100 (insulin lispro injection)
100 units/mL - Full Prescribing Information
Humalog® U-200 (insulin lispro injection)
200 units/mL - Full Prescribing Information
Humalog® MIX50/50™ (50% insulin lispro protamine suspension 50% insulin lispro injection [rDNA origin])
100 units/mL - Full Prescribing Information
Humalog® MIX75/25™ (75% insulin lispro protamine suspension 25% insulin lispro injection [rDNA origin])
100 units/mL
This information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
INSULIN LISPRO MIX75/25 Versus HUMALOG® MIX75/25
When transitioning from Humalog® Mix75/25™ to Insulin Lispro Protamine and Insulin Lispro Injectable Suspension Mix75/25™ KwikPen® (100 units/mL), no dose conversion is needed.
Do not perform dose conversion when transitioning to the generic LM75/25 3-mL Pen from Humalog Mix75/25 3-mL Pen.
For example, if a patient is transitioning from 20 units of Humalog Mix75/25, the patient would administer 20 units of generic LM75/25.
Generic LM75/25 is identical to Humalog Mix75/25 in terms of
active ingredients
inactive ingredients
manufacturing, and
3-mL Pen packaging.
Generic LM75/25 3-mL Pen has a unique NDC number, label, and package insert.
Enclosed Prescribing Information
INSULIN LISPRO PROTAMINE AND INSULIN LISPRO INJECTABLE SUSPENSION MIX75/25™, for subcutaneous use, Lilly
Glossary
Generic = authorized generic
Humalog Mix75/25 = Humalog® Mix75/25 (insulin lispro protamine and insulin lispro injectable suspension)
Lilly = Eli Lilly and Company
LM75/25 = Insulin Lispro Protamine and Insulin Lispro Injectable Suspension Mix75/25™
NDC = National Drug Code
Pen = KwikPen®
Date of Last Review: February 23, 2020
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