The first botulinum toxin product, onabotulinumtoxinA, was approved by the FDA in 1989. Since then, FDA has approved several ...
Parents and clinicians are urged to review usage of certain health products for young children after federal authorities ...
The Food and Drug Administration has issued 18 warning letters to online retailers selling unapproved and misbranded Botox ...
The FDA warning letters mostly went to cosmetic websites. In each case, the FDA said the companies were offering unofficial ...
This article was reviewed by Kelly Brown, MD. What Are the Best Male Enhancement Pills and Products? Ads for male enhancement ...
The head of the U.S. Food and Drug Administration’s drug division, Dr. George F. Tidmarsh, resigned on November 2, 2025, one ...
DSAP is a premalignant, progressive disease characterized by numerous expanding lesions which significantly impact quality-of ...
The U.S. FDA approved a pricey rare disease drug in September despite findings by its data reviewers that the treatment, ...
It is fair to say (no matter what else can be said) that the current administration is outcome- rather than process-driven. This general ...
The U.S. Food and Drug Administration issued 18 warning letters to owners of websites illegally marketing unapproved and misbranded botulinum toxin products, commonly called Botox. The agency is aware ...
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FDA to streamline approvals for generic biological drugs in latest move targeting health costs
The US Food and Drug Administration will take steps to streamline the process to develop generic versions of complex biological drugs, the agency announced Wednesday. The changes are meant to ...
The Food and Drug Administration (FDA) is launching an effort to streamline the approval process for cheaper alternative “biosimilar” versions of biologic drugs as a way to curb health costs. The ...
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