HERTFORDSHIRE, England and PITTSBURGH and BANGALORE, India, July 6, 2020 /PRNewswire/ -- Mylan N.V. (NASDAQ: MYL) today announced that the Drug Controller General of India (DCGI) has approved its ...

DUBLIN--(BUSINESS WIRE)--The "Lyophilized Drugs, Reconstitution Devices and Injection Markets: Products, Markets, Therapeutics, Strategies & Forecasts" report has been added to ...

Ilaris for Injection will be replaced by Ilaris Injection (solution) for subcutaneous use. The Food and Drug Administration (FDA) has posted that Ilaris (canakinumab; Novartis) lyophilized powder for ...

Zevtera is supplied as a single-dose vial containing 667mg of ceftobiprole medocaril sodium as a lyophilized powder for reconstitution. Zevtera ® (ceftobiprole medocaril sodium for injection) is now ...

The Gujarat Food and Drug Control Administration (FDCA) has issued test license to Hyderabad-based Hetero Labs to facilitate manufacturing of lyophilized injection of remdesivir drug meant for ...

Gufic Biosciences Limited’s shares were up by 2.31 per cent after the company received approvals from the Therapeutic Group Administration (TGA) in Australia and the National Health Surveillance ...

* MYLAN NV - DRUG IS APPROVED FOR TREATMENT OF SUSPECTED OR LABORATORY CONFIRMED INCIDENCES OF COVID-19 IN ADULTS AND CHILDREN Source text for Eikon: Further company coverage: ...