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- FDA’s Actions to Protect Children from Contaminated Cough Medicine
- FDA Approves Labeling Changes that Include a Boxed Warning for Immune Effector Cell-Associated Enterocolitis Following Treatment with Carvykti (ciltacabtagene autoleucel)
- FDA Removes Risk Evaluation and Mitigation Strategies (REMS) for Caprelsa (vandetanib)
- FDA Removes Risk Evaluation and Mitigation Strategy (REMS) Program for the Antipsychotic Drug Clozapine
- Unichem Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Cyclobenzaprine Hydrochloride Tablets USP 10 mg, Due to Mislabeling