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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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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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Zydus Gets US Regulator's Approval To Market Generic Epilepsy Drug
The drug will be manufactured at the group's formulation manufacturing facility at Ahmedabad SEZ, Zydus said in a statement.
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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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Marksans Pharma Shares Gain On USFDA Approval For Pain Killer Drug
Marksans will manufacture the products at its US Food and Drug Administration (USFDA) approved solid oral dosage facility located at Goa.
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Lupin Receives Tentative Nod For Anti-Seizure Drug; Stock Edges Higher
"The company (Lupin) has received tentative approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Brivaracetam Tablets," Lupin said
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Lupin Gains Nearly 1% As Subsidiary Gets New Drug Approval
The USFDA approved Lupin's US-based arm's supplemental new drug application (sNDA) to expand the use of Solosec for treating trichomoniasis in adults, Lupin said
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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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Strides Pharma Gets Nod For Prednisone Tablets; Stock Sheds Over 1%
Strides Pharma: Prednisone drugs, also known as corticosteroids, are used as anti-inflammatory and immuno-suppressant medications for treating allergic disorders, skin conditions, ulcerative colitis and arthritis.
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Glenmark Pharma Gets Regulatory Nod For Tacrolimus Capsules; Stock Gains Nearly 2%
Glenmark Pharma received final approval from USFDA for Tacrolimus capsules, which are used as immunosuppressants to prevent human immune system from rejecting liver, kidney and heart transplants.
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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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Strides Pharma Surges On USFDA Nod For Headache Drug
Strides Pharma shares surged as much as 5% after it got approval from USFDA for Butalbital, Acetaminophen, Caffeine, andCodeine Phosphate Capsules.
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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.
-
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.
-
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
-
Zydus Gets US Regulator's Approval To Market Generic Epilepsy Drug
The drug will be manufactured at the group's formulation manufacturing facility at Ahmedabad SEZ, Zydus said in a statement.
-
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
-
Marksans Pharma Shares Gain On USFDA Approval For Pain Killer Drug
Marksans will manufacture the products at its US Food and Drug Administration (USFDA) approved solid oral dosage facility located at Goa.
-
Lupin Receives Tentative Nod For Anti-Seizure Drug; Stock Edges Higher
"The company (Lupin) has received tentative approval from the United States Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Brivaracetam Tablets," Lupin said
-
Lupin Gains Nearly 1% As Subsidiary Gets New Drug Approval
The USFDA approved Lupin's US-based arm's supplemental new drug application (sNDA) to expand the use of Solosec for treating trichomoniasis in adults, Lupin said
-
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.
-
Strides Pharma Gets Nod For Prednisone Tablets; Stock Sheds Over 1%
Strides Pharma: Prednisone drugs, also known as corticosteroids, are used as anti-inflammatory and immuno-suppressant medications for treating allergic disorders, skin conditions, ulcerative colitis and arthritis.
-
Glenmark Pharma Gets Regulatory Nod For Tacrolimus Capsules; Stock Gains Nearly 2%
Glenmark Pharma received final approval from USFDA for Tacrolimus capsules, which are used as immunosuppressants to prevent human immune system from rejecting liver, kidney and heart transplants.
-
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.
-
Strides Pharma Surges On USFDA Nod For Headache Drug
Strides Pharma shares surged as much as 5% after it got approval from USFDA for Butalbital, Acetaminophen, Caffeine, andCodeine Phosphate Capsules.
-
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.
