FDA Approves oral pivmecillinam for Uncomplicated Urinary Tract Infections Dr. Kamal Kant Kohli25 April 2024 7:00 PM ISTThe U.S. Food and Drug Administration has approved oral pivmecillinam for the treatment of female adults with uncomplicated urinary tract infections...
Natco Pharma gets USFDA EIR on pharmacovigilance requirements Ruchika Sharma25 April 2024 5:44 PM ISTTelangana: Natco Pharma has informed in a BSE filing that the Company has received the Establishment Inspection Report (EIR) from the US Food and...
New treatment for Uncomplicated Urinary Tract Infections approved by FDA Roshni Dhar25 April 2024 5:16 PM ISTThe U.S. Food and Drug Administration has approved Pivya (pivmecillinam) tablets for the treatment of female adults with uncomplicated urinary tract...
Health Bulletin 25/ April/ 2024 Roshni Dhar25 April 2024 4:58 PM ISTHere are the top health news for the day:FDA approves new treatment for Uncomplicated Urinary Tract InfectionsThe Food and Drug Administration (FDA)...
GSK application for expanded indication of Jemperli plus chemotherapy accepted by USFDA for priority review Ruchika Sharma25 April 2024 12:40 PM ISTLondon: GSK plc has announced the US Food and Drug Administration (FDA) has accepted the supplemental Biologics License Application (sBLA) for...
Novartis radioligand therapy Lutathera gets USFDA nod for pediatric patients with gastroenteropancreatic neuroendocrine tumors Ruchika Sharma25 April 2024 12:14 PM ISTBasel: Novartis has announced that the U.S. Food and Drug Administration (FDA) has approved Lutathera (USAN: lutetium Lu 177 dotatate / INN:...
FDA fast tracks investigational gene therapy for heart failure Dr. Kamal Kant Kohli24 April 2024 7:30 PM ISTThe US Food and Drug Administration (FDA) has granted Fast Track designation to invesigational gene therapy AB-1002 for treatment of congestive heart...
USFDA issues 10 observations for Zydus Lifesciences Jarod facility Ruchika Sharma24 April 2024 4:01 PM ISTAhmedabad: Zydus Lifesciences has informed in a BSE filing that the US Food and Drug Administration (USFDA) has concluded an inspection with...
USFDA issues EIR for Lupin Aurangabad facility Ruchika Sharma24 April 2024 11:46 AM ISTMumbai: Global pharma major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States...
Zydus Lifesciences launches Mirabegron ER Tablets in US for overactive bladder treatment Ruchika Sharma22 April 2024 2:47 PM ISTMirabegron is indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency and urinary frequency.
Takeda gets USFDA nod for Entyvio subcutaneous administration for Crohn's disease Ruchika Sharma21 April 2024 10:00 AM ISTOsaka: Takeda has announced that the U.S. Food and Drug Administration (FDA) has approved ENTYVIO (vedolizumab) subcutaneous (SC)...
Roche Alecensa gets USFDA nod for ALK-positive early-stage lung cancer Ruchika Sharma20 April 2024 12:05 PM ISTBasel: Roche has announced that the U.S. Food and Drug Administration (FDA) has approved Alecensa (alectinib) for adjuvant treatment following...
