Search For "united states food and drug administration"
Zydus receives final approval from USFDA to market drug used to relieve ch
Updated : 4 years ago IST
New Delhi [India], March 9 (ANI): Zydus Lifesciences Ltd. has received final approval from the United States Food and Drug Administration (USFDA) to market Nitroglycerin Sublingual tablets used to relieve chest pain in people who have certain heart conditions, said the pharmaceutical company
Read More
Optimus receives tentative approval from U.S. FDA for Brexpiprazole Tablet
Updated : 4 years, 5 months ago IST
Hyderabad (Telangana) [India], October 9 (ANI/PNN): Optimus Pharma Private Limited today announced that it has received tentative approval from the United States Food and Drug Administration (FDA) for the generic equivalent of Rexulti® Tablets, 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, and 4 m
Read More
Covid antiviral pill cuts risk of hospitalisation, deaths by half, says ma
Updated : 4 years, 5 months ago IST
Washington [US], October 1 (ANI): An antiviral pill has been found to reduce the risk of hospitalisation and deaths by 50 per cent in patients diagnosed with COVID-19 during clinical trials.
Read More
Pfizer and BioNTech announce submission of Initial data to US FDA to suppo
Updated : 4 years, 7 months ago IST
New York [US], August 17 (ANI): Pfizer and BioNTech announced that they have submitted Phase 1 data to the United States Food and Drug Administration (FDA) to support the evaluation of a third, or booster dose of the companies' COVID-19 vaccine for future licensure.
Read More
We respect US FDA decision, but it won't impact India's vaccine plan: Cent
Updated : 4 years, 9 months ago IST
New Delhi [India], June 11 (ANI): Reacting to the United States Food and Drug Administration (FDA)'s rejection of Bharat Biotech's Covaxin jab for emergency use authorization, the Union Health Ministry on Friday said that it respects the decision taken by the authority but it will not hav
Read More
US FDA okays first new Alzheimer's drug in nearly 2 decades
Updated : 4 years, 9 months ago IST
Washington [US], June 8 (ANI): The United States Food and Drug Administration (FDA) has approved a new drug for Alzheimer's, the first new medicine against the disease in almost two decades.
Read More
Cipla receives final approval for generic version of GlaxoSmithKline's IMI
Updated : 5 years ago IST
Mumbai (Maharashtra) [India], March 2 (ANI/PRNewswire): Cipla Limited today announced that it has received final approval for its Abbreviated New Drug Application (ANDA) for Sumatriptan Nasal Spray, 20 mg from the United States Food and Drug Administration (U.S. FDA).
Read More
Glenmark Pharmaceuticals receives ANDA approval for Clindamycin Phosphate
Updated : 5 years, 1 month ago IST
Mumbai (Maharashtra) [India], February 11 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food and Drug Administration (U.S. FDA) for Clindamycin Phosphate Gel USP, 1 per cent, the generic version of Cleocin T® Gel, 1 per ce
Read More
US FDA authorises Moderna Covid-19 vaccine for emergency use
Updated : 5 years, 3 months ago IST
Washington [US], December 19 (ANI): The United States Food and Drug Administration's (FDA) on Friday (local time) has authorised Moderna coronavirus vaccine for emergency use for people aged 18 years and above.
Read More
US FDA approves remdesivir, first drug to treat COVID-19 patients
Updated : 5 years, 5 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
US authorises use of saliva test for COVID-19: FDA
Updated : 5 years, 7 months ago IST
Washington [US], August 16 (ANI/Sputnik): The United States' Food and Drug Administration (FDA) has approved a new COVID-19 testing method based on analysing saliva samples.
Read More
Cipla receives final approval for generic version of AstraZeneca Pharmaceu
Updated : 5 years, 12 months ago IST
Mumbai (Maharashtra) [India], Mar 27 (ANI/ PRNewswire): Cipla Limited (BSE: 500087) (NSE: CIPLA EQ) and hereafter referred to as "Cipla" today announced that it has received final approval for its Abbreviated New Drug Application (ANDA) for Esomeprazole for Oral Suspension 10mg, 20mg and 40m
Read More