For the symptomatic treatment of osteoarthritis and of joint discomfort.
What is it?
  • Glucosamine is an amino sugar that is a precursor for the synthesis of glycosaminoglycans such as hyaluronic acid, which is a component of most connective tissues and therefore vital for joint health.
  • It is a natural component of proteoglycans found in articular cartilage, intervertebral disc and synovial fluid.
  • The older we get, the more cartilage gradually deteriorates, causing pain and discomfort.
  • Glucosamine-API is considered a Symptomatic Slow Acting Drug for mild knee Osteoarthritis.
  • Clinical trials demonstrate it reduces joint pain and improves mobility.
  • Glucosamine supplied by Bioiberica is produced by hydrolysis of crustacean shells and is available for sale in the form of:
  • Glucosamine Hydrochloride
  • Glucosamine sulfate sodium chloride
  • Glucosamine sulfate potassium chloride
  • Bioiberica offers glucosamine as API for pharmaceuticals and nutraceutical quality glucosamine which is predominantly used as a main ingredient in nutraceutical and veterinary formulations.
  • Our Glucosamine is compliant with the most restrictive and up-to-date monographs (EP, USP and RP) and is GMP certified.
Product information
  • SOURCE: Exoskeletons of crustaceans.
  • SALTS:
    • Glucosamine hydrochloride
    • Glucosamine sodium sulfate
    • Glucosamine potassium sulfate
  • USES:
    • Pharmaceuticals
    • Nutraceuticals
  • QUALITIES: European, United States and Russian Pharmacopoeia.
  • DMFs/CERTIFICATIONS: DMF for all qualities, Halal and GMP certificates.
  • INDICATION: For the symptomatic treatment of mild knee osteoarthritis.
  • PRESENTATION: Powder, white to almost white.
  • RECOMMENDED DOSE: 1.500 mg/day
  • REGULATORY STATUS: Active Pharmaceutical Ingredient and Dietary Supplement Ingredient.
  • STORAGE AND PACKAGING: Store at room temperature. Packaged in a double bag in a 25 KG drum.
  • RE-ANALYSIS/EXPIRATION PERIOD: Re-analysis period of two years from the manufacture date.

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