Glenmark Pharmaceuticals’ Generic of Leo Pharma’s Enstilar Approved

Title: Glenmark Pharmaceuticals’ Generic Version of Leo Pharma’s Enstilar Receives Approval


Glenmark Pharmaceuticals has received approval from the US Food and Drug Administration (FDA) for its generic version of Leo Pharma’s Enstilar, a topical medication for the treatment of plaque psoriasis. This approval signifies a significant development in the availability and affordability of treatment options for patients with this chronic skin condition. In this blog, we will explore the key points surrounding Glenmark Pharmaceuticals’ approval of the generic version of Enstilar.

Key Points:

  1. Understanding Plaque Psoriasis and Enstilar Treatment:

Plaque psoriasis is a chronic autoimmune condition that results in the rapid buildup of skin cells, leading to red, itchy, and scaly plaques on the skin. Enstilar, developed by Leo Pharma, is a combination foam medication containing calcipotriene and betamethasone dipropionate. It is applied topically to reduce inflammation, control the rapid skin cell growth, and alleviate the symptoms associated with plaque psoriasis.

  1. Approval of Glenmark Pharmaceuticals’ Generic Version:

Glenmark Pharmaceuticals has received FDA approval to market and distribute a generic version of Enstilar, making it accessible to a wider patient population. Generic medications are bioequivalent to their brand-name counterparts, meaning they contain the same active ingredients, dosage form, strength, and route of administration. The approval of the generic version offers patients a more cost-effective alternative while maintaining comparable effectiveness.

  1. Increased Accessibility and Affordability of Treatment:

The approval of Glenmark Pharmaceuticals’ generic version of Enstilar brings potential benefits to patients with plaque psoriasis. By offering a generic option, the accessibility and affordability of the treatment are likely to improve. Generic medications often come at a lower cost compared to brand-name counterparts, making them more accessible to a broader range of patients and potentially reducing the financial burden associated with long-term treatment.

  1. Ensuring Safety and Quality in Generic Medications:

The FDA’s approval of the generic version of Enstilar assures patients and healthcare professionals that Glenmark Pharmaceuticals’ product meets the same rigorous standards of safety, effectiveness, and quality as the brand-name medication. The bioequivalence of the generic version ensures that patients can expect a comparable therapeutic outcome when switching from the brand-name to the generic treatment option.

  1. Importance of Generic Medications in Healthcare:

Generic medications play a crucial role in healthcare by increasing competition and driving down drug prices, leading to substantial cost savings for patients, healthcare providers, and insurance companies. The availability of generic versions provides options, promotes access to essential treatments, and allows for cost-savings that can be redirected towards other healthcare needs.


The approval of Glenmark Pharmaceuticals’ generic version of Enstilar represents a significant milestone in the treatment of plaque psoriasis. By providing an affordable alternative to the brand-name medication, this approval enhances accessibility to effective treatment options for patients living with this chronic skin condition. The availability of generic medications fosters competition, lowers drug costs, and contributes to the overall affordability and sustainability of healthcare. Glenmark Pharmaceuticals’ achievement in obtaining approval for its generic version of Enstilar brings hope for improved patient outcomes and better management of plaque psoriasis.