Aurobindo Pharma soars nearly 5% after US FDA's nod to its Gilenya Capsules
"Aurobindo Pharma Limited is pleased to announce that it has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Fingolimod Capsules, 0.5 mg, which is bioequivalent and therapeutically equivalent to the reference listed drug (RLD), Gilenya Capsules, 0.5 mg of Novartis Pharmaceuticals Corporation. The product will be launched in March 2024," said Aurobindo Pharma in a statement on Friday.
The approved product has an estimated market size of US$ 447.3 million for the twelve months ending January 2024, according to IQVIA. Photo: File/Representational