Zydus Cadila Gets Tentative Nod From U.S. FDA For Parkinson’s Treatment Capsule
Domestic pharma major Zydus Cadila, part of Cadila Healthcare Ltd. group, on Monday said it has received tentative approval from the U.S. health regulator for its generic version of Parkinson's disease treatment drug Carbidopa and Levodopa extended-release capsules.
The approval by the U.S. Food and Drug Administration is for Carbidopa and Levodopa extended-release capsules in the strengths of 23.75 mg/95 mg, 36.25 mg/145 mg, 48.75 mg/195 mg, and 61.25 mg/245 mg, Cadila Healthcare said in a regulatory filing.
This combination medication is indicated for the treatment of Parkinson's disease or Parkinson-like symptoms such as shakiness, stiffness, and difficulty moving and will be manufactured at the group's manufacturing facility at Special Economic Zone, Ahmedabad, it added.
The group now has 282 approvals and has so far filed over 386 abbreviated new drug applications since the commencement of the filing process in FY 2003-04, it said.