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Synchron Switch Now Lets You Control Your iPhone or iPad Using Brain: All Details
- Thursday November 3, 2022
- Written by Nithya P Nair, Edited by Siddharth Suvarna
Brain chip implant developer Synchron has created a device called 'Synchron Switch' that allows patients to control an iPhone or iPad using their brain. Synchron’s technology could lead to major advances and would change the day-to-day lives of people with severe disabilities.
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www.gadgets360.com
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Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
- Monday August 29, 2022
- India News | Press Trust of India
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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www.ndtv.com
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Zydus Cadila's US Firm Gets US Approval To Market Roflumilast Tablets
- Monday February 14, 2022
- World News | Press Trust of India
Cadlia Healthcare Ltd on Monday said group firm Zydus Pharmaceuticals (USA) Inc has received final approval from the US health regulator to market its generic version of Roflumilast tablets in the strength of 500 mcg indicated to reduce the risk of
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www.ndtv.com
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US Drug Regulator Recommends Emergency Approval Of Moderna Vaccine
- Friday December 18, 2020
- World News | Reuters
The US Food and Drug Administration (FDA) will "rapidly" work towards granting emergency approval of Moderna Inc's COVID-19 vaccine candidate, FDA Commissioner Stephen Hahn said on Thursday.
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www.ndtv.com
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US Gives Full Approval To Antiviral Drug Remdesivir To Treat COVID-19
- Friday October 23, 2020
- World News | Agence France-Presse
The US Food and Drug Administration on Thursday granted full approval to the antiviral drug remdesivir as a treatment for patients hospitalized with Covid-19, after conditional authorization was given in May.
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www.ndtv.com
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MDH Sambar Masala Fails US FDA Test, Three Lots Recalled: Make Everyday Masalas At Home (Recipes Inside)
- Thursday September 12, 2019
- Edited by Shubham Bhatnagar
The US Food and Drug Administration (US FDA) has found salmonella bacteria in MDH sambar masala, following which the products were recalled from the US earlier this week. Make everyday masalas at home with these easy recipes.
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food.ndtv.com
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Zydus Cadila Gets USFDA Nod To Drug That Treats Severe Acne Vulgaris
- Friday November 24, 2017
- Business | NDTV Profit Team
Zydus Pharmaceuticals has received the final approval from the USFDA to market Minocycline Hydrochloride Extended Release Tablets
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www.ndtv.com/business
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Synchron Switch Now Lets You Control Your iPhone or iPad Using Brain: All Details
- Thursday November 3, 2022
- Written by Nithya P Nair, Edited by Siddharth Suvarna
Brain chip implant developer Synchron has created a device called 'Synchron Switch' that allows patients to control an iPhone or iPad using their brain. Synchron’s technology could lead to major advances and would change the day-to-day lives of people with severe disabilities.
-
www.gadgets360.com
-
Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
- Monday August 29, 2022
- India News | Press Trust of India
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.
-
www.ndtv.com
-
Zydus Cadila's US Firm Gets US Approval To Market Roflumilast Tablets
- Monday February 14, 2022
- World News | Press Trust of India
Cadlia Healthcare Ltd on Monday said group firm Zydus Pharmaceuticals (USA) Inc has received final approval from the US health regulator to market its generic version of Roflumilast tablets in the strength of 500 mcg indicated to reduce the risk of
-
www.ndtv.com
-
US Drug Regulator Recommends Emergency Approval Of Moderna Vaccine
- Friday December 18, 2020
- World News | Reuters
The US Food and Drug Administration (FDA) will "rapidly" work towards granting emergency approval of Moderna Inc's COVID-19 vaccine candidate, FDA Commissioner Stephen Hahn said on Thursday.
-
www.ndtv.com
-
US Gives Full Approval To Antiviral Drug Remdesivir To Treat COVID-19
- Friday October 23, 2020
- World News | Agence France-Presse
The US Food and Drug Administration on Thursday granted full approval to the antiviral drug remdesivir as a treatment for patients hospitalized with Covid-19, after conditional authorization was given in May.
-
www.ndtv.com
-
MDH Sambar Masala Fails US FDA Test, Three Lots Recalled: Make Everyday Masalas At Home (Recipes Inside)
- Thursday September 12, 2019
- Edited by Shubham Bhatnagar
The US Food and Drug Administration (US FDA) has found salmonella bacteria in MDH sambar masala, following which the products were recalled from the US earlier this week. Make everyday masalas at home with these easy recipes.
-
food.ndtv.com
-
Zydus Cadila Gets USFDA Nod To Drug That Treats Severe Acne Vulgaris
- Friday November 24, 2017
- Business | NDTV Profit Team
Zydus Pharmaceuticals has received the final approval from the USFDA to market Minocycline Hydrochloride Extended Release Tablets
-
www.ndtv.com/business