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  2. Netarsudil/latanoprost - Wikipedia

    en.wikipedia.org/wiki/Netarsudil/latanoprost

    Netarsudil/latanoprost, sold under the brand name Rocklatan among others, is a fixed-dose combination medication use to treat elevated intraocular pressure (IOP) in people with open-angle glaucoma or ocular hypertension. It contains netarsudil mesylate and latanoprost. It is applied as eye drops to the eyes.

  3. Latanoprost - Wikipedia

    en.wikipedia.org/wiki/Latanoprost

    Latanoprost, sold under the brand name Xalatan among others, is a medication used to treat increased pressure inside the eye (intraocular pressure). This includes ocular hypertension and open-angle glaucoma. Latanaprost is applied as eye drops to the eyes. Onset of effects is usually within four hours, and they last for up to a day.

  4. Netarsudil - Wikipedia

    en.wikipedia.org/wiki/Netarsudil

    In the United States, in December 2017, the Food and Drug Administration (FDA) approved a 0.02% ophthalmic solution for the lowering of elevated intraocular pressure in people with open-angle glaucoma or ocular hypertension. The European Medicines Agency approved it in 2019 for the same uses under the brand name Rhokiinsa.

  5. Latanoprostene bunod - Wikipedia

    en.wikipedia.org/wiki/Latanoprostene_bunod

    Latanoprostene bunod (trade name Vyzulta) is an ophthalmic drug approved in the United States in 2017 for the reduction of intraocular pressure in patients with open-angle glaucoma or ocular hypertension.

  6. Ripasudil - Wikipedia

    en.wikipedia.org/wiki/Ripasudil

    Ripasudil (in the form of ripasudil hydrochloride hydrate) was approved by the PMDA of Japan on September 26, 2014. Glanatec, the trade name of the approved formulation, takes the form of an eye drop solution of 0.4% ripasudil, equivalent to 4 g of ripasudil per 1000 mL of solution.

  7. US FDA approves two biosimilars for blockbuster eye drug Eylea

    www.aol.com/news/us-fda-approves-two-biosimilars...

    US FDA approves two biosimilars for blockbuster eye drug Eylea. May 20, 2024 at 8:48 AM. (Reuters) -The U.S. Food and Drug Administration (FDA) on Monday approved two close copies of Regeneron ...