Is Lantus SoloSTAR 100 units/mL (insulin glargine) the same as other insulin glargine formulations?

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Last updated: October 15, 2026 • View editorial policy

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Yes, Lantus SoloSTAR 100 units/mL is insulin glargine

Lantus SoloSTAR 100 units/mL is the brand name for insulin glargine manufactured by Sanofi—they are the same medication. 1

Understanding the Product

Lantus is simply the brand name that Sanofi uses for their insulin glargine product. The SoloSTAR refers to the specific prefilled pen delivery device that contains this insulin. When you see "Lantus SoloSTAR 100 units/mL," this describes:

  • Lantus = Sanofi's brand name for insulin glargine
  • SoloSTAR = The disposable prefilled pen device
  • 100 units/mL (U-100) = The concentration of insulin glargine

The FDA-approved label explicitly states this is "insulin glargine injection" 1.

Important Distinctions to Understand

Different Concentrations of the Same Insulin

While Lantus SoloSTAR 100 units/mL and other insulin glargine products contain the same active ingredient (insulin glargine), there are clinically important differences between formulations:

  • U-100 glargine (Lantus): Standard concentration, available as vials and SoloSTAR pens 2
  • U-300 glargine (Toujeo): Three times more concentrated, has a longer duration of action but modestly lower efficacy per unit administered 3

These are NOT interchangeable unit-for-unit. U-300 glargine requires higher total daily doses to achieve equivalent glycemic control compared to U-100 4.

Biosimilar Products

Several biosimilar or follow-on products of insulin glargine U-100 are now available at lower costs 2, 5. These include products like Basaglar (LY IGlar) which have demonstrated similar pharmacokinetic and pharmacodynamic properties to Lantus in clinical trials 6, 7, 8. The 2025 ADA guidelines list these as "glargine follow-on products" with median costs of $118-$323 per 1,000 units compared to branded Lantus at $136 per 1,000 units 3.

Critical Safety Considerations

Never Mix or Substitute Without Medical Supervision

  • Do not mix insulin glargine with other insulins due to its low pH diluent 9, 1
  • Do not dilute or mix with any other solution 1
  • Any change between insulin types or manufacturers should occur under close medical supervision with increased glucose monitoring 3, 5

Dosing Errors to Avoid

  • Accidental mix-ups between insulin products can occur—always check insulin labels before injection 1
  • When switching between U-100 and U-300 formulations, expect to need different total daily doses to achieve the same glycemic control 3, 4
  • U-300 glargine showed patients required significantly more units daily than U-100 to achieve equivalent efficacy 4

Device-Specific Information

The SoloSTAR pen is a single-patient-use prefilled pen that should never be shared between patients, even if the needle is changed 1. After first use, store at room temperature below 86°F and discard after 28 days 1.

Clinical Equivalence of Biosimilars

Research demonstrates that biosimilar insulin glargine products have similar pharmacokinetic and pharmacodynamic profiles to Lantus. Studies show the 90% confidence intervals for all PK parameters (AUC, Cmax) fall within 80-125%, meeting regulatory requirements for biosimilarity 6, 8, 10. In clinical practice, these biosimilars provide comparable glucose control and safety to branded Lantus 7.

References

Research

Lilly Insulin Glargine Versus Lantus® in Insulin-Naïve and Insulin-Treated Adults with Type 2 Diabetes: A Randomized, Controlled Trial (ELEMENT 5).

Diabetes therapy : research, treatment and education of diabetes and related disorders, 2019

Guideline

insulin administration.

Diabetes Care, 2004

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.