Pharmaceutical Technology19 小时
FDA approves Alvotech and Teva’s SELARSDI for new indications
The FDA has approved a new presentation of Alvotech and Teva’s SELARSDI, for the treatment of ulcerative colitis and Crohn's ...
Novo Nordisk asks FDA to block compounding pharmacies from making Ozempic copy-cats
Novo Nordisk wants the Food and Drug Administration (FDA) to prevent compounding pharmacies from manufacturing their own ...
GlobalData on MSN2 天
FDA approves Astellas’ VYLOY for gastric cancer treatment
Astellas Pharma has gained approval from the US Food and Drug Administration (FDA) for VYLOY (zolbetuximab-clzb), in ...
The Pharma Letter16 小时
New FDA approval for Pfizer’s RSV vaccine Abrysvo
The US Food and Drug Administration (FDA) yesterday approved Abrysvo (respiratory syncytial virus vaccine). Developed and ...
The Pharma Letter1 天
FDA approves new presentation of biosimilar drug Selarsdi
Iceland-based Alvotech and the US unit of Israel’s of Teva Pharmaceutical Industries today revealed that that the US Food and ...
BioSpace15 小时
Novo Makes Case to FDA That Semaglutide Is Too Complex for Compounders to Produce
Novo Nordisk has nominated semaglutide for inclusion in the FDA’s Demonstrable Difficulties for Compounding list, which ...
FiercePharma14 小时
Novo Nordisk asks FDA to prevent compounders from making copycat versions of GLP-1 star ...
“Novo Nordisk’s aim with this nomination is to ensure that patients receive only FDA-approved, safe, and effective ...
MyJoyOnline3 天
Postinor 2 medicine with pink flower label is not approved – FDA
The Upper East Regional Office of the Food and Drugs Authority (FDA), says a type of Postinor 2 with a pink flower label on ...
Ozempic And Wegovy Maker Novo Nordisk Asks FDA To Halt Production Of Compounded Fat Loss ...
Novo Nordisk NVO has appealed to the U.S. Food and Drug Administration (FDA) to halt the production of compounded versions of ...
rheumatologyadvisor14 小时
FDA Approves Stelara Biosimilar Imuldosa
The FDA has approved Imuldosa, a biosimilar to Stelara (ustekinumab), for the treatment of various chronic inflammatory diseases.
Agri-Pulse23 小时
FDA, state feed officials seek new way to regulate ingredients
A Memorandum of Understanding between FDA and the Association of American Feed Control Officials, a group that represents ...
GlobalData on MSN5 天
Intercept’s liver disease drug Ocaliva faces FDA approval delay
An FDA AdCom in September recommended against full approval for Ocaliva by a 13-1 vote for the treatment of primary biliary ...