Off-brand versions of Lilly weight loss drug must be pulled off market, could mean higher prices
The United States Food and Drug Administration says the shortage of Eli Lilly’s Zepbound and Mounjaro drugs has been resolved ...
CBS News9d
FDA proposes new tests to detect asbestos in cosmetics and other products containing talc
a medical doctor and director of the FDA's Office of Cosmetics and Colors, said Thursday in a news release announcing the agency's action. The agency's proposed rule falls short of a ban on talc ...
FDA proposes new testing rules to ensure cosmetics are asbestos-free
The Food and Drug Administration is proposing a rule that cosmetic companies would have to take extra steps to ensure that ...
Verywell Health on MSN3d
Zepbound Gets FDA Approval to Treat Sleep Apnea
The obesity medication Zepbound can be used on-label to treat obstructive sleep apnea in adults with obesity, the FDA ...
The American Journal of Managed Care13d
FDA Approves First Generic Daily GLP-1 Injection for Type 2 Diabetes
The approval marks the second for a generic in this class of medications indicated to improve glycemic control in patients ...
Systane eye drops recalled for possible fungal contamination, FDA says
One lot of Systane Lubricant Eye Drops Ultra PF was recalled following a consumer complaint “of foreign material observed ...
The American Journal of Managed Care9d
5 Key Drug Approvals and CRLs in 2024
In 2024, multiple drugs received complete response letters (CRLs), sometimes unrelated to the safety and efficacy of the drug ...
Cingulate secures capital ahead of 2025 plans to submit drug for FDA approval
A KCK pharmaceutical company gets a cash injection that should sustain it long enough to get an ADHD drug to the FDA for ...
HealthDay on MSN2d
FDA approves Gemtesa for overactive bladder in men with BPH
Gemtesa is approved for men with overactive bladder symptoms who are receiving pharmacologic treatment for benign prostatic hyperplasia.
HealthDay on MSN13d
GLP-1 Zepbound Is Approved As First Drug For Sleep Apnea
The U.S. Food and Drug Administration (FDA) has approved the first prescription medication specifically for treating o ...
Cure Today13d
FDA Grants Breakthrough Therapy Designation to Trodelvy for Small Cell Lung Cancer
The FDA has granted breakthrough therapy designation Trodelvy for adults with extensive-stage small cell lung cancer who ...
Business Wire6d
Inogen Receives FDA 510(k) Clearance for SIMEOX 200 Airway Clearance Device
“We are very excited to receive FDA clearance for the innovative SIMEOX 200 therapy ... Forward-Looking Statements This press release contains forward-looking statements within the meaning of the ...