Search For "fda"
Updated : 1 day, 9 hours ago IST
Johannesburg [South Africa], April 14 (ANI): South African Health Minister Zweli Mkhize on Tuesday said that the country will be suspending the use of the Johnson & Johnson COVID-19 vaccine after health concerns raised by the US Food and Drug Administration (FDA).
Updated : 1 day, 19 hours ago IST
Washington [US], April 13 (ANI): The US Centers of Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA) have recommended "pause" in the use of Johnson and Johnson COVID-19 vaccine "out of an abundance of caution" over six reported cases in the US of a "rare and
Updated : 5 days, 12 hours ago IST
New York [US], April 10 (ANI): Pfizer and BioNTech requested the US Food and Drug Administration (FDA) on Friday for an amendment to its emergency use authorization of its Covid-19 vaccine, to expand its use for children ages 12 to 15 in the United States.
Updated : 1 week, 2 days ago IST
Washington [US], April 6, (ANI): The United States will still have enough vaccines for all Americans by the end of next month, despite problems with a single batch of "drug product" resulting in the loss of 15 million doses of Johnson & Johnson's vaccine, the White House said on Monday.
Updated : 1 week, 6 days ago IST
Washington [US], April 2 (ANI): Johnson and Johnson (J&J) vaccine supplier Emergent BioSolutions said in a statement that it acknowledges it botched a batch of vaccines but is confident of its ability to meet US government safety requirements and standards.
Updated : 2 weeks, 4 days ago IST
Washington [US], March 27 (ANI): The American multinational technology company, Amazon has received Food and Drug Administration authorization (FDA) for its COVID-19 test developed by its subsidiary STS Lab Holdco and the company is now intending to utilize it for its employee testing progra
Updated : 3 weeks, 1 day ago IST
Mumbai (Maharashtra) [India], March 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval from the United States Food & Drug Administration (US FDA) for Chlorpromazine Hydrochloride Tablets USP, 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg, the generic v
Updated : 3 weeks, 2 days ago IST
Mumbai (Maharashtra) [India], March 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Diltiazem Hydrochloride Extended-Release Capsules USP, 60 mg, 90 mg, and 120 mg, the generic ver
Updated : 4 weeks, 1 day ago IST
Washington [US], March 17 (ANI/Sputnik): The US government issued simplified rules for developers of coronavirus tests to promote serial screening, a process in which the same individual is tested multiple times within a few days, the Food and Drug Administration (FDA) said.
Updated : 1 month ago IST
Mumbai (Maharashtra) [India], March 11 (ANI): The Maharashtra Food and Drugs Administration (FDA) on Thursday said it is working to bring down the cost of the Remdesivir 100 mg injection, used for treating critical COVID-19 patients.
Washington DC [US], March 10 (ANI): 340 different coronavirus tests have so far won emergency use authorisation (EUA), including one that can be used at home without a prescription to detect the virus, the Food and Drug Administration (FDA) has said.
Updated : 1 month, 1 week ago IST
Washington [US], March 7 (ANI/Sputnik): Scientists at the US Food and Drug Administration (FDA) are strongly against administering only single doses of the Moderna and Pfizer vaccines, as their efficacy has only been proven if people get two shots, The Wall Street Journal reports.