Dimethyl fumarate DR capsules are a generic therapeutic equivalent of Biogen IDEC Inc’s Tecfidera. Both Glenmark and Cipla have the go ahead to market 120 mg and 240 mg formulations for the treatment of adults with relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease.

Sirolimus tablets are a generic version of PF Prism CV's rapamune tablets. They are prescribed to prevent rejection of kidney transplants either alone or in combination with other medications. The drug is a mammalian target of rapamycin (mTOR) inhibitor immunosuppressant and is not recommended for patients with lung or liver transplants. Glenmark will now be able to market 0.5 mg, 1 mg and 2 mg versions of the tablets.

Glenmark reported that, according to IQVIA sales data for the 12-month period ending August 2020, the market for Sirolimus achieved annual sales in the region of US$119.7 million and that of Tecfidera DR capsules reached US$3.8 billion. They also noted that their current portfolio consists of 165 products authorized for US distribution and they have 45 abbreviated new drug applications (ANDAs) pending approval.

Related articles
Mylan launches first generic of Tecfidera in the US

US patent office rules in Biogen’s favour on Tecfidera

Glenmark and Lupin gain FDA approval for nervous system agents

Three FDA approvals for Glenmark as it enters US branded dermatology market

Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.

Copyright – Unless otherwise stated all contents of this website are © 2020 Pro Pharma Communications International. All Rights Reserved.