Search For "drug administration"
US: FDA gives full approval to Pfizer-BioNTech COVID 19 vaccine
Updated : 4 years, 6 months ago IST
Washington [US] August 23 (ANI): The US Food and Drug Administration (FDA) on Monday gave full approval to Pfizer's COVID-19 vaccine.
Read More
Philippines approves Russia's Sputnik Light vaccine
Updated : 4 years, 6 months ago IST
Moscow [Russia], August 23 (ANI): The Philippines' Food and Drug Administration approved the single-component Sputnik Light coronavirus vaccine under the emergency use authorization procedure on Monday, the Russian Direct Investment Fund said.
Read More
Pfizer and BioNTech announce submission of Initial data to US FDA to suppo
Updated : 4 years, 6 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
Immunocompromised people in US to get 3rd dose of COVID-19 vaccines
Updated : 4 years, 7 months ago IST
Washington [US], August 13 (ANI/Sputnik): The US Food and Drug Administration (FDA) has authorized the emergency use of the third dose of both Moderna and Pfizer vaccines against COVID-19 for immunocompromised people.
Read More
Jubilant Pharma's rating headroom healthy despite import alert for India p
Updated : 4 years, 7 months ago IST
Singapore, July 26 (ANI): Jubilant Pharma Ltd (JPL) will continue to maintain good rating headroom as the impact of a recent US Food and Drug Administration import alert for its generic formulations plant in India will be limited, Fitch Ratings has said.
Read More
Nigeria approves Russia's Sputnik V COVID vaccine for use
Updated : 4 years, 8 months ago IST
Moscow [Russia], July 15 (ANI): The Russian Direct Investment Fund (RDIF) on Thursday announced the approval of the Russian Sputnik V vaccine against coronavirus by the National Agency for Food and Drug Administration and Control of Nigeria (NAFDAC).
Read More
FDA warns of rare neurological complication with J&J coronavirus vacci
Updated : 4 years, 8 months ago IST
Washington [US], July 13 (ANI): The US Food and Drug Administration (FDA) on Monday (local time) warned coronavirus vaccine maker Johnson & Johnson of possible rare neurological complications caused due to its dose.
Read More
Covid-19: Pfizer says it is time for booster dose, US govt officials say n
Updated : 4 years, 8 months ago IST
Washington [US], July 9 (ANI): US drugmaker Pfizer and Germany's BioNTech have announced that they will seek regulatory authorisation for a third dose of their Covid-19 vaccine.
Read More
US faces calls from experts to speed up COVID-19 vaccine approval process
Updated : 4 years, 8 months ago IST
Washington [US], June 28 (ANI): As the United States is poised to miss its July 4 goal of vaccinating 70 per cent of adult Americans, calls are rising from some experts for the Food and Drug Administration (FDA) to move faster to fully approve the COVID-19 vaccines as a key step to address v
Read More
Glenmark Pharmaceuticals receives ANDA tentative approval for Nintedanib C
Updated : 4 years, 8 months ago IST
Mumbai (Maharashtra) [India], June 25 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Nintedanib Capsules, 100 mg and 150 mg, the generic version of Ofev®1 Capsules, 100 mg and 1
Read More
Glenmark Pharmaceuticals receives ANDA approval for Arformoterol Tartrate
Updated : 4 years, 8 months ago IST
Mumbai (Maharashtra) [India], June 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Arformoterol Tartrate Inhalation Solution, 15 mcg/2 mL, Unit-Dose Vials, the generic version of BROVA
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