Dr Reddy’s Laboratories Ltd (DRL) has received approval from the US Food and Drug Administration (FDA) to launch doxorubicin hydrochloride liposome injection for intravenous use in the US market. DRL had partnered with Natco Pharma Ltd on R&D and manufacturing capabilities for developing the product, which is a generic version of Doxil (manufactured by Alza Corporation).
“This approval represents the first of its kind for Dr Reddy’s in the complex depot injectables arena. 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

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