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Dr Reddy’s Lab gets USFDA nod for Lenalidomide capsule

Dr Reddy’s Laboratories today said it has received approval from the US health regulator to market Lenalidomide capsules, used to treat multiple...

Bharat Biotech awaits DCGI nod to launch Covaxin for children

After getting approval from the Subject Expert Committee (SEC) for Covaxin to be used for children in the two-to-18 years of age...

Molbio gets DCGI nod for Truenat Scrub T test for Scrub...

Molbio Diagnostics, the innovator of Truenat, a point of care Real-Time PCR platform, received Drug Controller General of India (DCGI) approval for...

USFDA gives tentative nod to Gland Pharma for generic muscle relaxant...

Gland Pharma Limited, a generic injectable focused pharmaceutical company, received tentative approval from the United States Food and Drug Administration (USFDA) for...

USFDA gives tentative nod to Zydus Cadila for Adapalene and Benzoyl...

Zydus Cadila has received tentative approval from the US Food and Drugs Administration (USFDA) to market Adapalene and Benzoyl Peroxide Gel 0.3%/2.5%....

USFDA gives nod to Drug to treat Rare Autoimmune Disease

ChemoCentryx Inc said on Friday the U.S. health agency approved its lead drug for treating a rare, fatal autoimmune disease, sending the biopharmaceutical...

USFDA gives tentative nod to Lupin for generic Brexpiprazole tablets

Lupin yesterday said it has received tentative nod from the US health regulator to market generic Brexpiprazole tablets, which are used with...

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CDSCO to enhance testing capacity for Medical Devices

The Drugs Controller General of India (DCGI) is in the process of enhancing capacity for testing medical devices in the country in...

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