The FDA refers to the Food and Drug Administration. Most states in India have their own FDA which is responsible for the quality of food and pharmaceutical products available in the state. The term is also used on our site to describe the United States FDA which is becoming more and more active with Indian pharma companies entering the US market.
The recalled was initied by the Oregon Potato Company LLC on 12 February due to risk of Listeria contamination.
FDA approves evidence-based tool (Bysanti) to address severe mood and psychotic symptoms, which may predict future indications.
Officially launched in 2015, FDA has approved the first-ever gastric balloon that helps reduce body weight by 14 per cent.
The United States Food and Drug Administration (FDA), firstly initiated the recall in April 2025 and Class II Classification was further implemented on February 12 until further notice.
According to the University of Georgia's Health Centre, there are two types of whey protein, including isolate and concentrate, the former of which is typically "a highly filtered form of whey protein and contain less than 1% of lactose."
To take cognizance of the situation, FDA said this week that the company that makes the glucose monitor has directed distributors and health care providers to remove FreeStyle Libre 3 Sensor and FreeStyle Libre 3 Plus Sensor from where they're sold.
The U.S. Food and Drug Administration has recalled over 580,000 bottles of a blood-pressure drug after finding a potentially cancer-causing chemical impurity.
One of the studies has found that there is a possibility of cockroaches in pre-ground coffee.
The US Food and Drug Administration (FDA) has approved the first-ever blood test to diagnose the debilitating Alzheimer's disease early.
Nearly half of Karnataka's local ice cream, ice candy, and cool drink manufacturing units have been flagged by the Food Safety and Drug Administration Department (FDA) for selling substandard products under unhygienic conditions.
US FDA has approved its first ever non-opioid painkiller called suzetrigine. Experts believe it will prevent addiction problems unlike existing opioids.
While talc is a naturally-occurring mineral that is used in cosmetics, asbestos, a known carcinogen, is said to be inseparable from talc in the mining process.
Despite the availability of Xolair, people are advised to continue avoiding foods that cause them reactions -- mostly peanuts, walnuts, hazelnuts, cashews, milk products and eggs.
The FDA has issued an expanded warning against purchasing or using certain eyedrops.
According to recent reports, USA has officially approved the manufacture of the first oral pill to treat postpartum depression.
How much is your immunity against covid? Now you can test it with this immunity test kit.
The U.S. Food and Drug Administration (FDA) has identified around 77 hand sanitizers as dangerous for health. Read on to know more.
Researchers have identified 21 existing drugs that can stop the replication of SARS-CoV-2, the virus that causes COVID-19. Four of these drugs can improve the activity of remdesivir.
The FDA has approved a new drug for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia with a FLT3 mutation.
The U.S. Food and Drug Administration found that in most of the cases the presence of such ingredients was not noted anywhere on supplement labelling. While some products cited the warnings, especially the weight-loss products the other conveniently ignored it.
Diabetes impairs the body's ability to make or properly use the blood glucose-regulating hormone insulin.
The new gene therapy will treat retinal dystrophy caused by a specific genetic mutation.
Here's why the US FDA decided that consumer antiseptic wash products containing certain active ingredients can no longer be marketed in the country.
Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the U.S. Food and Drug Administration (FDA) granted accelerated approval to Tecentriq (atezolizumab) for the treatment of people with locally advanced or metastatic urothelial carcinoma (mUC) who have disease progression during or following platinum-based chemotherapy.
The recalled was initied by the Oregon Potato Company LLC on 12 February due to risk of Listeria contamination.
FDA approves evidence-based tool (Bysanti) to address severe mood and psychotic symptoms, which may predict future indications.
Officially launched in 2015, FDA has approved the first-ever gastric balloon that helps reduce body weight by 14 per cent.
The United States Food and Drug Administration (FDA), firstly initiated the recall in April 2025 and Class II Classification was further implemented on February 12 until further notice.
According to the University of Georgia's Health Centre, there are two types of whey protein, including isolate and concentrate, the former of which is typically "a highly filtered form of whey protein and contain less than 1% of lactose."
To take cognizance of the situation, FDA said this week that the company that makes the glucose monitor has directed distributors and health care providers to remove FreeStyle Libre 3 Sensor and FreeStyle Libre 3 Plus Sensor from where they're sold.
The U.S. Food and Drug Administration has recalled over 580,000 bottles of a blood-pressure drug after finding a potentially cancer-causing chemical impurity.
One of the studies has found that there is a possibility of cockroaches in pre-ground coffee.
The US Food and Drug Administration (FDA) has approved the first-ever blood test to diagnose the debilitating Alzheimer's disease early.
Nearly half of Karnataka's local ice cream, ice candy, and cool drink manufacturing units have been flagged by the Food Safety and Drug Administration Department (FDA) for selling substandard products under unhygienic conditions.
US FDA has approved its first ever non-opioid painkiller called suzetrigine. Experts believe it will prevent addiction problems unlike existing opioids.
While talc is a naturally-occurring mineral that is used in cosmetics, asbestos, a known carcinogen, is said to be inseparable from talc in the mining process.
Despite the availability of Xolair, people are advised to continue avoiding foods that cause them reactions -- mostly peanuts, walnuts, hazelnuts, cashews, milk products and eggs.
The FDA has issued an expanded warning against purchasing or using certain eyedrops.
According to recent reports, USA has officially approved the manufacture of the first oral pill to treat postpartum depression.
How much is your immunity against covid? Now you can test it with this immunity test kit.
The U.S. Food and Drug Administration (FDA) has identified around 77 hand sanitizers as dangerous for health. Read on to know more.
Researchers have identified 21 existing drugs that can stop the replication of SARS-CoV-2, the virus that causes COVID-19. Four of these drugs can improve the activity of remdesivir.
The FDA has approved a new drug for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia with a FLT3 mutation.
The U.S. Food and Drug Administration found that in most of the cases the presence of such ingredients was not noted anywhere on supplement labelling. While some products cited the warnings, especially the weight-loss products the other conveniently ignored it.
Diabetes impairs the body's ability to make or properly use the blood glucose-regulating hormone insulin.
The new gene therapy will treat retinal dystrophy caused by a specific genetic mutation.
Here's why the US FDA decided that consumer antiseptic wash products containing certain active ingredients can no longer be marketed in the country.
Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the U.S. Food and Drug Administration (FDA) granted accelerated approval to Tecentriq (atezolizumab) for the treatment of people with locally advanced or metastatic urothelial carcinoma (mUC) who have disease progression during or following platinum-based chemotherapy.
