Natco gets USFDA nod for Carfilzomib Injection

The parties have received final approval for 10 mg and 60 mg strengths of the product and tentative approval for 30 mg strength of the product.

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USFDA
Picture: Pixabay

Last Updated on June 16, 2021 by The Health Master

Natco Pharma announced that its marketing partner, Breckenridge Pharmaceutical has received approval for its Abbreviated New Drug Application (ANDA) for Carfilzomib Vials ANDA (generic for KYPROLIS), from the US Food and Drug Administration (USFDA).

Medicine Injection drug vaccine
Picture: Pixabay

The parties have received final approval for 10 mg and 60 mg strengths of the product and tentative approval for 30 mg strength of the product. Based on the ANDA filing date NATCO believes that it is eligible for 180 days of sole generic marketing exclusivity for the 10 mg strength and shared 180 days of generic marketing exclusivity for the 60 mg strength of the product at the time of launch.

In the year 2019, the parties have reached a Settlement Agreement on para IV litigation related to the product with Onyx Therapeutics. By virtue of the settlement, NATCO and Breckenridge have been granted a license permitting the launch of their generic carfilzomib products on a date that is held as confidential in the year 2027 or sooner depending on certain occurrences.

As per industry sales data, KYPROLIS had generated annual sales of $696 million during the twelve months ending December 2020 in the US. 10mg strength alone generated sales of $63 million for the same period.

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