Glenmark Pharma arm secures USFDA nod for Ryaltris nasal spray
Mumbai: Glenmark Pharmaceuticals Limited, a research-led, global integrated pharmaceutical company announced that its fully owned subsidiary Glenmark Specialty S.A. (Switzerland), received US Food and Drug Administration (USFDA) approval on its New Drug Application (NDA) for Ryaltris, an innovative, fixed dose (metered), prescription, combination drug product nasal spray for the treatment of symptoms of Seasonal Allergic Rhinitis in adults and pediatric patients 12 years of age and older in the United States.
The recommended daily dose for Ryaltris is 2 sprays in each nostril twice daily.
"The FDA's approval of Ryaltris represents a major milestone for Glenmark and clearly supports our efforts to bring innovative treatment options in our key therapeutic areas." said Mr. Robert Crockart Chief Commercial Officer of Glenmark Pharmaceuticals Limited.
"With this NDA approval, we look forward to bringing this new medicine to physicians and their patients for the treatment of symptoms of seasonal allergic rhinitis, including nasal and ocular symptoms."
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