Mylan FDA Wednesday, June 19, 2019 0.00 Neutral

FDA Approves SCOPOLAMINE — Mylan Pharmaceuticals Inc.

Mylan received FDA approval on June 19, 2019, for the generic transdermal formulation of scopolamine, signaling a significant opportunity for market expansion into the motion-sickness sector. This approval for ANDA203753 is expected to provide intense competitive pressure on brand competitors by offering more affordable access to this chronic OTC treatment.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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