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Dr. Reddy s Laboratories announces USFDA approval for the launch of Doxorubicin Hydrochloride Liposome Injection in the U.S. Market Hyderabad, India

Key Takeaway: Hyderabad, India and Princeton, NJ, USA. May 17 2017 Dr. Reddy s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY) announced today that it has received approval from the U.S. Food and Drug Administration (USFDA) to launch Doxorubicin Hydrochloride Liposome Injection, a th

Full Press Release Details

Hyderabad, India and Princeton, NJ, USA. May 17 2017 Dr. Reddy s
Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY) announced today that it has received approval from the U.S. Food and Drug Administration (USFDA) to launch Doxorubicin Hydrochloride Liposome Injection, a therapeutic equivalent generic
version of Doxil (doxorubicin hydrochloride liposome injection), for intravenous use, in the United States market. USFDA approval is an outcome of extensive collaboration with the
company s partner, Natco Pharma Ltd. (NSE: NATCOPHARM; BSE: 524816), on R&D and manufacturing capabilities.
represents the first of its kind for Dr. Reddy s in the complex depot injectables arena, explains Alok Sonig, Executive Vice President and Head of the North America Generics business at Dr. Reddy s Laboratories. It is
a testament to our commitment to bring affordable generic medicines to market for patients. The approval further validates our capabilities to successfully develop and manufacture complex liposomal formulations. We are preparing for a
commercial launch soon.
We are pleased with our partnership with Dr.Reddy s Laboratories. This approval would not have
been possible without their guidance and support, says Rajeev Nannapaneni, Vice Chairman and Chief Executive Officer, Natco Pharma.
The Doxil brand and generic had U.S. sales of approximately $196 million MAT
for the most recent twelve months ending in March 2017 according to IMS Health*.
Dr. Reddy s Doxorubicin Hydrochloride Liposome
Injection is a sterile, translucent, red liposomal dispersion in 10-mL or 30-mL glass, single-dose vials. Each 10-mL vial
contains 20 mg doxorubicin hydrochloride at a concentration of 2 mg/mL. Each 30-mL vial contains 50 mg doxorubicin hydrochloride at a concentration of 2 mg/mL. The following individually cartoned vials are
mg in vial fill volume vial size
20 mg vial 10-mL 10-mL
50 mg vial 25-mL 30-mL
WARNING: CARDIOMYOPATHY and INFUSION RELATED REACTIONS
See full prescribing information for complete boxed warning.
DOXIL is a registered trademark of ALZA
*IMS National Sales Perspective: Retail and Non-Retail MAT March 2017
About Dr. Reddy s : Dr. Reddy s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY) is an integrated pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses Pharmaceutical Services & Active Ingredients, Global Generics and Proprietary Products Dr. Reddy s offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Our major therapeutic areas of focus are gastrointestinal, cardiovascular, diabetology, oncology, pain management and dermatology. Dr. Reddy s operates in markets across the globe. Our major markets include USA, India, Russia & CIS countries, and Europe. For more information, log on to: www.drreddys.com
Disclaimer : This press release may include statements of future expectations and other forward-looking statements that are based on the management s current views and assumptions and involve known or unknown risks and uncertainties that could cause actual results, performance or events to differ materially from those expressed or implied in such statements. In addition to statements which are forward-looking by reason of context, the words may , will , should , expects , plans , intends , anticipates , believes , estimates , predicts , potential , or continue and similar expressions identify forward-looking statements. Actual results, performance or events may differ materially from those in such statements due to without limitation, (i) general economic conditions such as performance of financial markets, credit defaults, currency exchange rates, interest rates, persistency levels and frequency / severity of insured loss events (ii) mortality and morbidity levels and trends, (iii) changing levels of competition and general competitive factors, (iv) changes in laws and regulations and in the policies of central banks and/or governments, (v) the impact of acquisitions or reorganization, including related integration issues. The company assumes no obligation to update any information contained herein.
Last updated: May 17, 2017