(a) Specifications.
        
        (1) 
         Each 1-milliliter (mL) ampule of solution contains 250 milligrams (mg) polysulfated glycosaminoglycan.
     
    
        
        (2) 
         Each mL of solution packaged in 5-mL ampules or 20-, 30-, or 50-mL vials contains 100 mg polysulfated glycosaminoglycan.
     
    
        
        (b) Sponsor.
         See No. 010797 in  § 510.600(c) of this chapter.
     
    
        
        (c) Special considerations.
         Federal law restricts this drug to use by or on the order of a licensed veterinarian.
     
    
        
        (d) Conditions of use—
        
        (1) Horses—
         For the treatment of noninfectious degenerative and/or traumatic joint dysfunction and associated lameness of the carpal and hock joints in horses.
     
    
        
        (ii) Amount—
        
        (A) Intra-articular use (carpal):
         250 mg once a week for 5 weeks.
     
    
        
        (B) Intramuscular use (carpal and hock):
         500 mg every 4 days for 28 days.
     
    
        
        (iii) Limitations.
         Do not use in horses intended for human consumption.
     
    
        
        (2) Dogs—
        
        (i) Indications for use.
         For control of signs associated with noninfectious degenerative and/or traumatic arthritis of canine synovial joints.
     
    
        
        (ii) Amount.
         2 mg per pound of body weight by intramuscular injection twice weekly for up to 4 weeks (maximum of 8 injections).
     
    
        
            Code of Federal Regulations
        
        [72 FR 56896, Oct. 5, 2007, as amended at 74 FR 67816, Dec. 21, 2009]