United States Food And Drugs Administration

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Adulterated Drugs On Decline Amid Crackdown

Rise in raids on illicit drug manufacturing units, alongside arrests for the production, sale, or distribution of spurious or adulterated drugs. Photograph: Yves Herman/Reuters The......

Diabetes Drug Linked To Vision Loss?

Study suggested that constant use of Semaglutide may be linked to development of a condition called non-arteritic ischemic optic neuropathy. IMAGE: Kindly note the image has been posted only for......

A COVID-19 Vaccine Snapshot

Sputnik V is already approved in India and Sinovac is unlikely to come in as it does not meet the criteria, reports Sohini Das. IMAGE: A woman receives a dose of Covishield at a vaccination centre......

US FDA warns against side effects of malaria drug

The United States Food and Drug Administration has issued a safety communication regarding the known side effects of anti-malarial drug hydroxychloroquine, touted by President Donald Trump for......

Molnupiravir not to be included in Covid treatment now

The Indian Council of Medical Research's national task force for COVID-19 has decided against including antiviral drug Molnupiravir in the clinical management protocol for COVID-19 as of now,......

Indian food, drugs 2nd on US refusal list

Even though India does not figure among the top trade partners of the United States, its food and medicines have attracted the second highest number of import refusals from the US. With 1,610 cases......

'Real growth and opportunity are going to come from GLP-1'

'It is not just the US and European opportunity, but it is a huge global opportunity.' Photograph: Kind courtesy Biocon The peptides and GLP-1 class of drugs that are offering breakthrough......

Ranbaxy gets US FDA nod for drug

Ranbaxy Laboratories on Monday said it has received tentative approval from the United States Food and Drug Administration to manufacture and market anti-hypertension drug Quinapril Hydrochloride......

Cadila gets tentative FDA nod

Cadila Healthcare Ltd has received tentative approval from the United States Food and Drug Administration to market Pravastatin Sodium Tablets in the US market.The tentative approval was given for......

Ranbaxy gets nod for Fluoxetine

United States' Food and Drug Administration has granted approval to Ranbaxy Laboratories Ltd to manufacture and market 40 mg capsules of Fluoxetine, a drug used in treatment of obsessive-compulsive......

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United States Food And Drugs Administration

News for United States Food And Drugs Administration

Adulterated Drugs On Decline Amid Crackdown

Diabetes Drug Linked To Vision Loss?

A COVID-19 Vaccine Snapshot

US FDA warns against side effects of malaria drug

Molnupiravir not to be included in Covid treatment now

Indian food, drugs 2nd on US refusal list

'Real growth and opportunity are going to come from GLP-1'

Ranbaxy gets US FDA nod for drug

Cadila gets tentative FDA nod

Ranbaxy gets nod for Fluoxetine

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