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Tag: US FDA

You Searched For "US FDA"
FDA approves Jardiance for heart failure in adults

FDA approves Jardiance for heart failure in adults

Dr. Kamal Kant Kohli24 Feb 2022 8:24 PM GMT
The U.S. Food and Drug Administration has approved diabetes drug Jardiance for heart failure in adults. This will help reduce the risk of...
USFDA nod to Zydus to market generic version of Vigabatrin

USFDA nod to Zydus to market generic version of Vigabatrin

Dr. Divya Colin21 Jan 2022 10:32 AM GMT
The approval by the US Food and Drug Administration is for Vigabatrin tablets of 500 mg strength, Cadila Healthcare said in a regulatory filing.
Merck to supply 3 million doses of molupiravir to UNICEF

Merck to supply 3 million doses of molupiravir to UNICEF

Dr. Divya Colin20 Jan 2022 12:32 PM GMT
Merck , known as MSD outside the United States and Canada, and Ridgeback Biotherapeutics announced the signing of a long-term supply agreement...
FDA Approves Glycopyrrolate Orally Disintegrating Tablets for peptic ulcer

FDA Approves Glycopyrrolate Orally Disintegrating Tablets for peptic ulcer

Hina Zahid23 Dec 2021 3:30 AM GMT
PARSIPPANY, N.J. - The Food and Drug Administration has granted approval for Dartisla ODT (glycopyrrolate) in adults to reduce symptoms of a peptic...
FDA Approves tofacitinib for Treatment of Active Ankylosing Spondylitis

FDA Approves tofacitinib for Treatment of Active Ankylosing Spondylitis

Hina Zahid20 Dec 2021 3:30 AM GMT
NEW YORK - The U.S. Food and Drug Administration (FDA) has approved the supplemental New Drug Application (sNDA) for XELJANZ® / XELJANZ® XR...
FDA panel backs molnupiravir-  first at-home COVID-19 pill

FDA panel backs molnupiravir- first at-home COVID-19 pill

Medha Baranwal2 Dec 2021 5:15 AM GMT
USA: The Food and Drug Administration's (FDA's) antimicrobial drugs advisory committee has concluded that potential benefits of Merck's molnupiravir...
MRI safety software tool receives FDAs qualification for MDDT

MRI safety software tool receives FDA's qualification for MDDT

Medha Baranwal29 Nov 2021 3:30 AM GMT
USA: The US Food and Drug Administration (FDA) has given the regulatory go-ahead to a software tool designed to help users analyze the safety of MRI...
FDA approves new Drug for Early Breast Cancer

FDA approves new Drug for Early Breast Cancer

Dr. Kamal Kant Kohli14 Oct 2021 2:09 PM GMT
The US food and drug administration has approved a new drug abemaciclib for one type of breast cancer. FDA has s approved Abemaciclib in...
FDA panel recommends Pfizer COVID booster for seniors, high-risk groups

FDA panel recommends Pfizer COVID booster for seniors, high-risk groups

Medha Baranwal19 Sep 2021 4:10 PM GMT
USA: A panel of The Food and Drug Administration (FDA) advisors has approved a third booster dose of Pfizer-BioNTech's COVID-19 vaccine on an...
FDA approves twice yearly injection for treatment for adults with schizophrenia

FDA approves twice yearly injection for treatment for adults with schizophrenia

Hina Zahid3 Sep 2021 4:45 AM GMT
USA: The U.S. Food and Drug Administration (FDA) has approved Invega Hafyera (paliperidone palmitate), the first-and-only twice-yearly injectable for...
FDA approves novel rehabilitation system for stroke victims

FDA approves novel rehabilitation system for stroke victims

Dr Kartikeya Kohli28 Aug 2021 3:45 AM GMT
The U.S. Food and Drug Administration has approved first-of-its-kind, drug-free rehabilitation system intended to treat moderate to severe upper...
FDA approves drug for chronic, excessive sleepiness during daytime

FDA approves drug for chronic, excessive sleepiness during daytime

Dr. Kamal Kant Kohli13 Aug 2021 2:45 AM GMT
The US Food and Drug Administration has approved a new indication for Xywav for idiopathic hypersomnia (IH) in adults. Xywav (calcium, magnesium,...
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