Zydus Cadila To Make Gilead's Potential COVID-19 Drug Remdesivir
Remdesivir, intravenously administered in hospitals, has already been approved for emergency use in severely-ill patients in the United States, India and South Korea.13-06-2020
Zydus Cadila To Make Gilead's Potential COVID-19 Drug Remdesivir
Remdesivir, intravenously administered in hospitals, has already been approved for emergency use in severely-ill patients in the United States, India and South Korea.CADILA HEALTHCARE LTD. - 532321 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Zydus signs a non exclusive licensing agreement with Gilead Sciences Inc., to manufacture and market RemdesivirCADILA HEALTHCARE LTD. - 532321 - Announcement under Regulation 30 (LODR)-Newspaper Publication
Newspaper publicationCADILA HEALTHCARE LTD. - 532321 - Large Corporate
Disclosure with regard to Large CorporateCADILA HEALTHCARE LTD. - 532321 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Zydus Cadila receives final approval from USFDA for Atazanavir CapsulresCadila Healthcare share price rises 3% on EIR from USFDA
The USFDA had conducted an inspection at the facility from 2 to 9 March, 2020.Three employees of Cadila Pharmaceuticals die of coronavirus in Gujarat
Ahmedabad district, which is worst-hit by the coronavirus pandemic, so far recorded 9,724 cases and 645 deathsZydus Cadila supplies 30,000 COVID KAVACH Elisa test kits to ICMR
The kits, to be used for antibody detection of Covid-19, have been manufactured in collaboration (via technology transfer) with ICMR-NIV of Pune for surveillance purposesCADILA HEALTHCARE LTD. - 532321 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
Zydus supplies first batch of 30,000 COVID KAVACH ELISA tests to ICMR, free of cost