This site is intended for healthcare professionals
Latest drug news
  • Home
  • /
  • News
  • /
  • 2022
  • /
  • 2
  • /
  • Viatris is first to receive FDA approval of generi...
News

Viatris is first to receive FDA approval of generic Restasis (cyclosporine ophthalmic emulsion 0.05%) to treat dry eye disease.

Read time: 1 mins
Published:5th Feb 2022
Viatris Inc. announced that its subsidiary, Mylan Pharmaceuticals Inc., has received approval from the FDA for its Abbreviated New Drug Application (ANDA) for Cyclosporine Ophthalmic Emulsion 0.05%, the first generic version of Allergan's Restasis. There are no remaining legal or regulatory barriers, and the company is launching immediately.

Cyclosporine Ophthalmic Emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca, also known as dry eye. Dry eye disease is a common condition that occurs when a patient's tears are unable to provide adequate lubrication for their eyes. Tears can be inadequate and unstable for many reasons, but the instability can lead to discomfort, inflammation and potential damage of the eye's surface.

Condition: Dry Eye Disease
Type: drug

Learning Zones

The Learning Zones are an educational resource for healthcare professionals that provide medical information on the epidemiology, pathophysiology and burden of disease, as well as diagnostic techniques and treatment regimens.