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Lupin launches new generic drug in US market
Pharma major Lupin Limited announced on Monday that it has launched Mirabegron extended-release tablets, 25 mg, in the United States market, after...
After UK, US FDA approves 2 gene therapies to treat sickle-cell...
The US Food and Drug Administration on Saturday approved two cell-based gene therapies -- Casgevy and Lyfgenia -- to sickle cell disease (SCD)...
Gland Pharma surges 3.6% after US FDA inspection at Hyderabad
Gland Pharma shares surged by 3.64% on the NSE to reach Rs 1769.90 at 10:57 am on November 24, following the receipt of the Establishment Inspection...
Granules gets USFDA nod for hypertension drug
Hyderabad-headquartered pharmaceutical major Granules India Limited announced that the US Food and Drug Administration (US FDA) has approved its...
T-Hub hosts US FDA delegation
The visit was centered around exploring the innovation ecosystem with a focus on MedTech, Healthcare and Innovation
US FDA approves drug to prevent RSV
The US Food and Drug Administration (FDA) on Tuesday approved a drug to prevent Respiratory Syncytial Virus (RSV) in children aged up to 24 months who...
Granules gets FDA nod for ache relieving drug
Pharmaceutical major headquartered in Hyderabad, Granules India Limited on Friday announced that the US Food and Drug Administration (US FDA) has...
Granules India completes US FDA audits at Visakhapatnam and...
The Vizag facility was inspected by the US FDA from June 26 to June 30, 2023 and the Jeedimetla facility from June 19 to June 23, 2023
