By: Sarah Ibrahim, PhD, Associate Director of Stakeholder and Global Engagement, Office of Generic Drugs, CDER CDER’s Office of Generic Drugs (OGD) and the European Medicines […]
MedWatch, the FDA’s medical product safety reporting program for health professionals, patients and consumers. MedWatch receives reports from the public and when appropriate, publishes safety alerts […]
By: Sarah Ibrahim, PhD, Associate Director of Stakeholder and Global Engagement, Office of Generic Drugs, CDER CDER’s Office of Generic Drugs (OGD) and the European Medicines […]
For Immediate Release: February 06, 2024 Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: On Monday, […]
Tianeptine is not approved by the U.S. Food and Drug Administration for any medical use. Despite that, some companies are illegally marketing and selling products containing […]
Delivery Method: VIA UPS Reference #: 320-24-18 Product: Drugs Recipient: Recipient Name Mr. Patrick Toledano Recipient Title President Les Importations Herbasanté Inc. 377 Sainte-Croix AveSaint-Laurent QC […]
Reference #: WL 2642 Product: Drugs Issuing Office: Center for Drug Evaluation and Research | CDER United States Secondary Issuing Offices United States WARNING LETTER February […]
Delivery Method: VIA EMAIL WITH READ RECEIPT Product: Drugs Recipient: Recipient Name Mr. Sunan Ge Recipient Title Site Manager Nantong Furuida Packaging Products Co., Ltd. No […]
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