Wexford announces approval of In Vitro Bioequivalence

Metformin is a widely prescribed medication used for the management of type 2 diabetes, a chronic disease that affects millions of people worldwide. It is an essential tool for controlling blood sugar levels and improving the overall health and well-being of individuals with diabetes.

In vitro bioequivalence testing of Metformin is a crucial step in the ongoing pursuit of excellence in the pharmaceutical industry. It ensures that generic versions of the medication are equivalent to the brand-name products they aim to replace, providing healthcare providers and patients with confidence in their safety and effectiveness.

Wexford Laboratories, Inc. spared no effort in conducting comprehensive and meticulous in vitro studies to demonstrate the bioequivalence of their Metformin product. The results of these studies have now been verified and validated by leading experts in the field, confirming that Wexford’s Metformin is truly bioequivalent to the reference medication.

Thomas Factor, President of Wexford Laboratories, commented that this significant achievement underscores Wexford Laboratories, Inc.’s unwavering commitment, stating, “Our mission has been and will continue to be manufacturing high-quality pharmaceutical products for the industry’s best companies.”

Wexford Laboratories, Inc. remains committed to maintaining the highest standards of quality and efficacy in its products. The successful conclusion of in vitro bioequivalence testing for Metformin reflects the company’s dedication to advancing diabetes care through innovation and research.

For more information about Wexford Laboratories, Inc. and its range of products for diabetes management, please visit www.wexlabs.com or contact our media relations department at media@wexlabs.com.

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