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Apple Receives US FDA Approval to Enable AirPods Pro 2 Hearing Aids Feature
AirPods Pro (2nd Generation) users will be able to use the company's truly wireless stereo (TWS) headset as a hearing aid in the future, as Apple has now received approval from the US Food and Drug Administration (FDA) to enable the feature. An update will also bring support for a new hearing test, which will generate an audio profile for the heari...
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Elon Musk's Neuralink Gets Go Ahead For Brain Chip Implant In 2nd Patient: Report
The US health regulator has allowed billionaire Elon Musk's Neuralink to implant its brain chip in a second person after it proposed to fix a problem that occurred in its first patient, the Wall Street Journal reported on Monday.
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US Approves First Drug For People With Severe Form Of Fatty Liver Disease
The US Food and Drug Administration (FDA) on Thursday approved the first medication for people with a severe type of non-alcoholic fatty liver disease.
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Miracle Drug That Could Extend Dogs' Lives Inches Closer to Approval
A medication with the potential to prolong the lifespans of large dogs and contribute to their overall health in aging is nearing its market debut.
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Opinion: Would You Let Elon Musk Implant A Device In Your Brain?
Elon Musk's Neuralink received approval last week from the US Food and Drug Administration to conduct human clinical trials, which one former FDA official called "really a big deal."
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Elon Musk's Neuralink Says It Has FDA Approval for Study of Brain Implants in Humans
Elon Musk's brain-implant company Neuralink on Thursday said the US Food and Drug Administration (FDA) had given the green light to its first-in-human clinical trial, a critical milestone after earlier struggles to gain approval.
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Zydus Gets US Regulator's Approval For Blood Pressure Medication
Zydus Lifesciences on Thursday said it received final approval from the US Food and Drug Administration (FDA) to manufacture and market Metoprolol Tartrate tablets in dosages of 25 mg, 50 mg, and 100 mg
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Alembic Pharma Gets Regulator's Approval To Market Antidepressant Drug In US
Alembic Pharmaceuticals has received an approval from the US Food & Drug Administration to market Brexpiprazole tablets in strengths of 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg and 4 mg.
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Neuralink Expected to Begin Human Clinical Trials in Six Months, Elon Musk Says
Neuralink is expected to begin human trials in six months, Elon Musk said on Wednesday. The brain chip interface is running behind schedule, and is said to have repeatedly missed internal deadlines to gain US Food and Drug Administration (FDA) approval to start human trials. Over a year ago, Neuralink demonstrated its technology on a monkey with a ...
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Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
Lupin on Monday said it has received a tentative approval from the US health regulator to market Dasatinib tablets, used to treat certain types of cancer, in America.
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FDA Announces All Juul E-Cigarettes, Vaping Products Off Market Over Safety Concerns
The US Food and Drug Administration has ordered all vaping products produced by Juul Labs off the market after finding the former industry leader had failed to address certain safety concerns. Juul was blamed for a surge in youth vaping over its marketing of fruit and candy flavored e-cigarettes.
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Dr Reddy's Laboratories Gets FDA Approval, Launches Drug In US Market
Dr Reddy's Laboratories on Wednesday said it has launched a vasopressin injection, which is used to control frequent urination, increased thirst, and loss of water caused by diabetes, in the American market.
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US Gives Full Approval To Moderna's COVID-19 Vaccine For Adults
The US Food and Drug Administration (FDA) announced Monday that it has granted full approval to Moderna's COVID19 "Spikevax" vaccine, which had previously received an emergency use authorization in the United States.
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Zydus Cadila Gets Final Approval From US FDA For Pre-Surgery Injection
India-based pharma giant, Zydus Cadila received final approval from US Food and Drug Administration (FDA) for Glycopyrrolate injection that is used before surgery to decrease the volume of secretions from the mouth, lungs and stomach.
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Lupin Gains On Receiving US FDA Nod To Launch Drug For Onychomycosis
Lupin received approval to launch Tavaborole Topical Solution, 5 per cent in United States (US) from the United States Food and Drug Administration (FDA).
-
Apple Receives US FDA Approval to Enable AirPods Pro 2 Hearing Aids Feature
AirPods Pro (2nd Generation) users will be able to use the company's truly wireless stereo (TWS) headset as a hearing aid in the future, as Apple has now received approval from the US Food and Drug Administration (FDA) to enable the feature. An update will also bring support for a new hearing test, which will generate an audio profile for the heari...
-
Elon Musk's Neuralink Gets Go Ahead For Brain Chip Implant In 2nd Patient: Report
The US health regulator has allowed billionaire Elon Musk's Neuralink to implant its brain chip in a second person after it proposed to fix a problem that occurred in its first patient, the Wall Street Journal reported on Monday.
-
US Approves First Drug For People With Severe Form Of Fatty Liver Disease
The US Food and Drug Administration (FDA) on Thursday approved the first medication for people with a severe type of non-alcoholic fatty liver disease.
-
Miracle Drug That Could Extend Dogs' Lives Inches Closer to Approval
A medication with the potential to prolong the lifespans of large dogs and contribute to their overall health in aging is nearing its market debut.
-
Opinion: Would You Let Elon Musk Implant A Device In Your Brain?
Elon Musk's Neuralink received approval last week from the US Food and Drug Administration to conduct human clinical trials, which one former FDA official called "really a big deal."
-
Elon Musk's Neuralink Says It Has FDA Approval for Study of Brain Implants in Humans
Elon Musk's brain-implant company Neuralink on Thursday said the US Food and Drug Administration (FDA) had given the green light to its first-in-human clinical trial, a critical milestone after earlier struggles to gain approval.
-
Zydus Gets US Regulator's Approval For Blood Pressure Medication
Zydus Lifesciences on Thursday said it received final approval from the US Food and Drug Administration (FDA) to manufacture and market Metoprolol Tartrate tablets in dosages of 25 mg, 50 mg, and 100 mg
-
Alembic Pharma Gets Regulator's Approval To Market Antidepressant Drug In US
Alembic Pharmaceuticals has received an approval from the US Food & Drug Administration to market Brexpiprazole tablets in strengths of 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg and 4 mg.
-
Neuralink Expected to Begin Human Clinical Trials in Six Months, Elon Musk Says
Neuralink is expected to begin human trials in six months, Elon Musk said on Wednesday. The brain chip interface is running behind schedule, and is said to have repeatedly missed internal deadlines to gain US Food and Drug Administration (FDA) approval to start human trials. Over a year ago, Neuralink demonstrated its technology on a monkey with a ...
-
Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
Lupin on Monday said it has received a tentative approval from the US health regulator to market Dasatinib tablets, used to treat certain types of cancer, in America.
-
FDA Announces All Juul E-Cigarettes, Vaping Products Off Market Over Safety Concerns
The US Food and Drug Administration has ordered all vaping products produced by Juul Labs off the market after finding the former industry leader had failed to address certain safety concerns. Juul was blamed for a surge in youth vaping over its marketing of fruit and candy flavored e-cigarettes.
-
Dr Reddy's Laboratories Gets FDA Approval, Launches Drug In US Market
Dr Reddy's Laboratories on Wednesday said it has launched a vasopressin injection, which is used to control frequent urination, increased thirst, and loss of water caused by diabetes, in the American market.
-
US Gives Full Approval To Moderna's COVID-19 Vaccine For Adults
The US Food and Drug Administration (FDA) announced Monday that it has granted full approval to Moderna's COVID19 "Spikevax" vaccine, which had previously received an emergency use authorization in the United States.
-
Zydus Cadila Gets Final Approval From US FDA For Pre-Surgery Injection
India-based pharma giant, Zydus Cadila received final approval from US Food and Drug Administration (FDA) for Glycopyrrolate injection that is used before surgery to decrease the volume of secretions from the mouth, lungs and stomach.
-
Lupin Gains On Receiving US FDA Nod To Launch Drug For Onychomycosis
Lupin received approval to launch Tavaborole Topical Solution, 5 per cent in United States (US) from the United States Food and Drug Administration (FDA).
