Dr Reddy’s gets USFDA nod for Azacitidine injection

Our Bureau Updated - March 12, 2018 at 09:28 PM.

Pharma major Dr Reddy’s Laboratories Ltd has received approval from the United States Food & Drug Administration (USFDA) for its Azacitidine injection.

This is a bioequivalent generic version of VIDAZA (Azacitidine for injection) and is indicated in the treatment of some types of cancer and disorders that affect the bone marrow.

The launch of the product in the market is planned in the near-term, the Hyderabad-based company said in a release on Tuesday.

The VIDAZA brand had US sales of approximately $378.5 million for the most recent 12 months ending July 2013, according to IMS Health.

Published on September 17, 2013 07:18