Usfda Approval
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New Diabetes Generic Drug Gets Approval In US Market: All About Dapagliflozin
Zydus Lifesciences has received USFDA approval for generic dapagliflozin tablets used to treat type 2 diabetes. Here's how the drug works, its benefits, and why it is important for blood sugar control and heart health.
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US Approves Lab-Grown Chicken To Be Sold In Markets, Twitter Reacts
The United States Department of Agriculture (USDA) has granted approvals to two companies selling chicken grown from animal cells.
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Synchron Switch Now Lets You Control Your iPhone or iPad Using Brain: All Details
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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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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Zydus Cadila's US Firm Gets US Approval To Market Roflumilast Tablets
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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US Drug Regulator Recommends Emergency Approval Of Moderna Vaccine
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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US Gives Full Approval To Antiviral Drug Remdesivir To Treat COVID-19
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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MDH Sambar Masala Fails US FDA Test, Three Lots Recalled: Make Everyday Masalas At Home (Recipes Inside)
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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Zydus Cadila Gets USFDA Nod To Drug That Treats Severe Acne Vulgaris
Zydus Pharmaceuticals has received the final approval from the USFDA to market Minocycline Hydrochloride Extended Release Tablets
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Cipla Receives USFDA's Final Approval For Generic Dacogen
Cipla has received final approval for its ANDA for Decitabine Injection 50 mg single-use sterile vial from the US FDA
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New Diabetes Generic Drug Gets Approval In US Market: All About Dapagliflozin
Zydus Lifesciences has received USFDA approval for generic dapagliflozin tablets used to treat type 2 diabetes. Here's how the drug works, its benefits, and why it is important for blood sugar control and heart health.
-
US Approves Lab-Grown Chicken To Be Sold In Markets, Twitter Reacts
The United States Department of Agriculture (USDA) has granted approvals to two companies selling chicken grown from animal cells.
-
Synchron Switch Now Lets You Control Your iPhone or iPad Using Brain: All Details
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.
-
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.
-
Zydus Cadila's US Firm Gets US Approval To Market Roflumilast Tablets
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
-
US Drug Regulator Recommends Emergency Approval Of Moderna Vaccine
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.
-
US Gives Full Approval To Antiviral Drug Remdesivir To Treat COVID-19
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.
-
MDH Sambar Masala Fails US FDA Test, Three Lots Recalled: Make Everyday Masalas At Home (Recipes Inside)
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.
-
Zydus Cadila Gets USFDA Nod To Drug That Treats Severe Acne Vulgaris
Zydus Pharmaceuticals has received the final approval from the USFDA to market Minocycline Hydrochloride Extended Release Tablets
-
Cipla Receives USFDA's Final Approval For Generic Dacogen
Cipla has received final approval for its ANDA for Decitabine Injection 50 mg single-use sterile vial from the US FDA
