Search For "drug administration"
340 different COVID-19 tests approved so far in US
Updated : 5 years ago IST
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.
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FDA warns against one-dose regimen for coronavirus vaccines
Updated : 5 years 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.
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Hygiene-related lapses found at 5-star hotel in Mumbai, kitchen store seal
Updated : 5 years ago IST
Mumbai (Maharashtra) [India], March 5 (ANI): Maharashtra's Food and Drug Administration (FDA) has found hygiene-related lapses in a five-star hotel in Bandra and sealed the store of its kitchen.
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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).
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Johnson & Johnson COVID vaccine approval is 'exciting' but US cannot '
Updated : 5 years ago IST
Washington [US], February 28 (ANI): US President Joe Biden on Saturday said the approval of Johnson & Johnson's single-shot coronavirus vaccine by the US Food and Drug Administration (FDA) is "exciting news" but warned Americans against letting their guard down as the situation could det
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US FDA panel gives go-ahead to Johnson & Johnson's COVID-19 vaccine
Updated : 5 years ago IST
Washington [US], February 27 (ANI): A US Food and Drug Administration (FDA) advisory panel on Friday endorsed Johnson & Johnson's coronavirus vaccine and recommended the agency grant emergency authorisation.
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Johnson & Johnson's single-dose COVID-19 vaccine meets requirements fo
Updated : 5 years ago IST
Washington [US], February 24 (ANI): The US Food and Drug Administration said on Wednesday that Johnson and Johnson's single-dose COVID-19 vaccine has met the requirements for emergency use authorisation.
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Maharashtra has ample medical supply for second COVID-19 wave, says state
Updated : 5 years ago IST
Mumbai (Maharashtra) [India], February 24 (ANI): The Maharashtra Food and Drug Administration (FDA) on Wednesday clarified that the state has ample medicines and other medical supplies in case of a second COVID-19 wave.
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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
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US approves emergency use of Eli Lilly's antibody cocktail for COVID-19 tr
Updated : 5 years, 1 month ago IST
Washington [US], February 10 (ANI): The US Food and Drug Administration (FDA) has granted an emergency use authorization to a monoclonal antibody cocktail made by pharmaceutical company Eli Lilly for treating coronavirus patients at high risk of developing severe COVID-19.
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Glenmark Pharmaceuticals receives ANDA approval for Topiramate Extended-re
Updated : 5 years, 1 month ago IST
Mumbai (Maharashtra) [India], February 3 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Topiramate Extended-Release Capsules, 25 mg, 50 mg, 100 mg, 150 mg, and 200 mg, the generic ve
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Glenmark Pharmaceuticals receives ANDA approval for Amphetamine Sulfate Ta
Updated : 5 years, 1 month ago IST
Mumbai (Maharashtra) [India], January 29 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Amphetamine Sulfate Tablets USP, 5 mg and 10 mg, the generic version of Evekeo®1 Tablets,
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