Merz North America has received the green light from the Food and Drug Administration for Xeomin (incobotulinumtoxinA) for the treatment of chronic sialorrhea, or excessive drooling, in adult patients.
Albertsons pharmacies were given agency approval to pilot Idaho’s new prescribing authority, which took effect July 1, making it the first large retail chain pharmacy in the nation to offer these expanded services.
Drug firm Zydus Cadila has received the Food and Drug Administration’s nod for generic Adalat CC (nifedipine extended-release tablets), and for generic Questran (cholestyramine for oral suspension).
Key factors in the decision included comments noting that the number of reference product lots biosimilar developers would need to purchase under the draft guidance if it were finalized could impact cost and efficiency.