FDA will periodically update a publicly available list of MUMS-designated drugs. This list will be placed on file at the FDA Division of Dockets Management, and will contain the following information for each MUMS-designated drug:
    
    
        
        (a) 
         The name and address of the sponsor;
     
    
        
        (b) 
         The established name and trade name, if any, of the drug;
     
    
        
        (c) 
         The dosage form of the drug;
     
    
        
        (d) 
         The species and the proposed intended use for which MUMS-drug designation was granted; and
     
    
        
        (e) 
         The date designation was granted.