Search For "drug administration"
FDA panel nod to emergency use approval for Pfizer vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 11 (ANI): A panel of experts advising the US Food and Drug Administration (FDA) on Thursday recommended emergency approval for the Pfizer-BioNTech Covid-19 vaccine.
Read More
COVID-19: Moderna submits vaccine data to obtain emergency use authorisati
Updated : 5 years, 3 months ago IST
Washington DC [US], December 1 (ANI): US biotech company Moderna said that it has submitted the results of its coronavirus vaccine trials to the country's Food and Drug Administration (FDA) in order to obtain emergency use authorisation for the vaccine.
Read More
Moderna to request Emergency use authorisation, its vaccine 100% effective
Updated : 5 years, 3 months ago IST
Washington [US], November 30 (ANI): US biotech company Moderna on Monday announced that it plans to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and conditional approval from the European Medicines Agency (EMA) after the final results from a lat
Read More
Pfizer, BioNTech to submit to FDA for emergency use authorisation for thei
Updated : 5 years, 3 months ago IST
Washington [US], November 20 (ANI): American drug giant Pfizer and German laboratory BioNTech on Friday said that they will be submitting to the US Food and Drug Administration for emergency use authorisation for their COVID-19 vaccine candidate.
Read More
IIT Roorkee scientists predict FDA-approved commercial drugs through AI to
Updated : 5 years, 4 months ago IST
Roorkee (Uttarakhand) [India], November 13 (ANI): Amid the rapid transmission of cases of Covid-19, a group of scientists from IIT Roorkee has leveraged Artificial Intelligence (AI) to predict 10 FDI (Food and Drug Administration) approved commercial drugs available for the treatment of the
Read More
Glenmark Pharmaceuticals receives ANDA approval for Tacrolimus Capsules US
Updated : 5 years, 4 months ago IST
Mumbai (Maharashtra) [India], November 11 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc., USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (U.S. FDA) for Tacrolimus Capsules USP, 0.5 mg, 1 mg and 5 mg, the generic version of Prograf®1 C
Read More
US allows emergency use of Eli Lilly's COVID-19 antibody treatment
Updated : 5 years, 4 months ago IST
Washington DC [US], November 10 (ANI): The US Food and Drug Administration (FDA) has approved an emergency use authorisation (EUA) for American pharmaceutical company Eli Lilly's experimental COVID-19 antibody treatment called 'bamlanivimab' for non-hospitalised patients with mild-to-moderat
Read More
AstraZeneca resumes US COVID-19 vaccine trial
Updated : 5 years, 4 months ago IST
London [UK], October 24 (ANI): The clinical trials for the AstraZeneca Oxford coronavirus vaccine -- AZD1222 -- have resumed in the United States after approval by the Food and Drug Administration (FDA), the company said on Friday (local time).
Read More
US FDA approves remdesivir, first drug to treat COVID-19 patients
Updated : 5 years, 4 months ago IST
Washington [US], October 23 (ANI): The United States Food and Drug Administration (FDA) has approved Remdesivir for the treatment of coronavirus, Al Jazeera reported citing a statement issued by Gilead Sciences, Inc.
Read More
Glenmark Pharmaceuticals receives ANDA approval for Sirolimus tablets, 0.5
Updated : 5 years, 4 months ago IST
Mumbai (Maharashtra) [India], Oct 19 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has received final approval by the United States Food & Drug Administration (US FDA) for Sirolimus Tablets, 0.5 mg, 1 mg and 2 mg, the generic version of Rapamune®1 Tablets, 0.5 mg, 1
Read More
Glenmark Pharmaceuticals receives ANDA approval for Dimethyl Fumarate Dela
Updated : 5 years, 5 months ago IST
Mumbai (Maharashtra) [India] October 7 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has been granted final approval by the United States Food & Drug Administration (US FDA) for Dimethyl Fumarate Delayed-Release Capsules, 120 mg and 240 mg, the generic version of Tecfide
Read More
Credit metrics of leading pharma companies to remain stable: ICRA
Updated : 5 years, 5 months ago IST
New Delhi [India], Sep 26 (ANI): The global demand scenario for Indian pharmaceutical industry is largely expected to remain stable due to inelastic nature of prescription drugs, investment information agency ICRA has said.
Read More