Active Ingredient: Hyaluronate Sodium Presentation: Liquid Strength: 10 mg/ml NDC Number: 00010-4705-20
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Indicated in the treatment of joint dysfunction of the carpus or fetlock in horses due to noninfectious synovitis associated with equine osteoarthritis.

  • Pure hyaluronic acid
  • Only FDA-approved joint therapy for both IV and IA administration
  • Up to three, once weekly IV doses will treat all affected fetlocks and carpi of the horse

Active Ingredient: Hyaluronate Sodium Presentation: Liquid Strength: 10 mg/ml NDC Number: 00010-4705-20 Color Of Medicine: Clear Container Type: Vial Delivery Type: Injection Reconstitution Required: N NDC Number: 00010-4705-20