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                Animal Drugs
                Sierra and a sister company, Veterinary Pharmaceuticals, Inc., signed the consent decree, agreeing t...
                
                
             
                            
                                    
                                    
                Animal Drugs
                In a 3/15 editorial, the increasingly influential newspaper cited a European Union ban on subtherape...
                
                
             
                            
                                    
                                    
                Medical Devices
                FDA grants a humanitarian-use device designation to Cyberkinetics Neurotechnology Systems for its An...
                
                
             
                            
                                    
                                    
                FDA General
                From a long FDA career of massaging regulated industry into compliance  --  sometimes a little rough...
                
                
             
                            
                                    
                                    
                FDA General
                Consulting editor John Scharmann receives an FOI response from FDA that is five years late and says ...
                
                
             
                            
                                    
                                    
                Human Drugs
                FDAs Oncologic Drugs Advisory Committee votes to not recommend approval for a Genta NDA for leukemia...
                
                
             
                            
                                    
                                    
                Human Drugs
                Like its parent corporation, Schering, a week before it, now Berlex Labs has received a Warning Lett...
                
                
             
                            
                                    
                                    
                Human Drugs
                With electronic submission standards and processes in place, FDA's Center for Drug Evaluation and Re...
                
                
             
                            
                                    
                                    
                Human Drugs
                Parkinson's disease patients whose medications for their movement disorders often cause psychotic sy...
                
                
             
                            
                                    
                                    
                Human Drugs
                FDA has approved a Duramed ANDA for oxycodone with acetaminophen capsules, 5mg/500mg. The company sa...
                
                
             
                            
                                    
                                    
                Human Drugs
                Adolor Corp. says FDA has accepted its IND for use of ADL 10-0101, a peripheral nervous system-selec...
                
                
             
                            
                                    
                                    
                Human Drugs
                FDA 3/1/99 approved an Apotex ANDA suitability petition for foscarnet sodium injection, 12mg/ml, 250...
                
                
             
                            
                                    
                                    
                Human Drugs
                CDC says FDA has helped manufacturers prepare to ship a record volume of flu vaccine this season.
                
                
             
                            
                                    
                                    
                Human Drugs
                Merck's cholesterol-lowering drug Mevacor (lovastatin) has gained an additional indication  --  redu...
                
                
             
                            
                                    
                                    
                Human Drugs
                FDA is giving manufacturers of over-the-counter analgesic/antipyretic drug products until 10/22 inst...
                
                
             
                            
                                    
                                    
                Medical Devices
                Boston Scientific acknowledges an internal study found an increased risk of late stent thrombosis wi...
                
                
             
                            
                                    
                                    
                Federal Register
                Federal Register Notice: FDA releases a draft guidance on frequently asked questions about commercia...
                
                
             
                            
                                    
                                    
                Human Drugs
                FDA has drafted procedures for drug and biologic sponsors to follow in requesting formal meetings to...
                
                
             
                            
                                    
                                    
                Human Drugs
                Pharmaceutical Research and Manufacturers (PhRMA) and the American Academy of Pediatrics have filed ...
                
                
             
                            
                                    
                                    
                Human Drugs
                An appeal to FDA OMBudsman AmANDA Norton by Stephen D. Mumford, a shipper of quinacrine for non-surg...