Search For "us fda"
Evidence of COVID-19 originating from Chinese lab continues to grow: Forme
Updated : 4 years, 10 months ago IST
Washington [China], May 25 (ANI): The former head of the US Food and Drug Administration (FDA) on Monday said that circumstantial evidence of COVID-19 originating in a lab in China's Wuhan continues to grow as researchers are yet to prove that the virus jumped from an animal to humans, The H
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US FDA approves emergency use of Pfizer-BioNTech vaccine for children in 1
Updated : 4 years, 10 months ago IST
Washington [US], May 11 (ANI): The US Food and Drug Administration (FDA) on Monday (local time) authorised the emergency use of the Pfizer-BioNTech COVID-19 vaccine to children in the age group of 12-15 years.
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Centre issues regulatory pathways for foreign-produced COVID-19 vaccines
Updated : 4 years, 11 months ago IST
New Delhi [India], April 15 (ANI): In view of the rapid surge in coronavirus cases in India, the Central government approved a significant streamlining and fast-tracking of the regulatory system for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which ar
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Health Ministry issues regulatory pathways for foreign-produced COVID-19 v
Updated : 4 years, 11 months ago IST
New Delhi [India], April 15 (ANI): The Central Government on Thursday issued the regulatory pathway in India for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency Use Listing (EUL), said the Union Health Ministry.
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Glenmark Pharmaceuticals receives ANDA approval for Chlorpromazine Hydroch
Updated : 5 years 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
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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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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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Glenmark launches SUTIB (Sunitinib) - priced 96% lower than the innovator
Updated : 5 years, 1 month ago IST
Mumbai (Maharashtra) [India], February 16 (ANI/PRNewswire): Glenmark Pharmaceuticals, a research-led, global integrated pharmaceutical company, today launched SUTIB, the generic version of Sunitinib oral capsules to treat kidney cancer in India.
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Glenmark's consolidated net profit rises by 30.05% to Rs. 2481.79 Mn. in Q
Updated : 5 years, 1 month ago IST
Mumbai (Maharashtra) [India], February 13 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited, a research-led global integrated pharmaceutical company, today announced its financial results for the third quarter ended December 31 of the financial year 2020-21.
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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 FDA probing 'about five' allergic reactions to Pfizer COVID-19 vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 19 (ANI/Sputnik): The US Food and Drug Administration (FDA) is probing roughly five instances of individuals having allergic reactions to Pfizer and BioNTech's vaccine against COVID-19, Peter Marks, the director of the FDA's Center for Biologics Evaluation and Resea
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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.
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