Aurobindo Pharma gets final USFDA nod for dementia drug
New Delhi : Drug firm Aurobindo Pharma BSE -2.11 % has received final approval from USFDA to manufacture and market Rivastigmine Tartrate Capsules USP, used for the treatment of dementia disease, in the American market.
"The company has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Rivastigmine Tartrate Capsules USP, 1.5 mg, 3 mg, 4.5 mg and 6 mg," Aurobindo Pharma said in a BSE filing.
The company said this product is expected to be launched in the first quarter of next fiscal.
The approved product is bioequivalent and therapeutically equivalent to Novartis Pharmaceuticals Corporation's Exelon Capsules, it added.
According to IMS, the approved product has an estimated market size of USD 26.7 million for the twelve months ending January 2016, Aurobindo Pharma said.
Exelon is used in the treatment of mild moderate dementia of the Alzheimer's and Parkinson's disease.
Aurobindo Pharma currently has a total of 246 ANDA approvals (211 final approvals including 10 from Aurolife Pharma LLC and 35 tentative approvals) from the US.
Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd