DOLENIO

This brand name is authorized in Cyprus, Estonia, France, Ireland, Lithuania, Malta, Netherlands, Poland, UK.

Active ingredients

The drug DOLENIO contains one active pharmaceutical ingredient (API):

1
UNII N08U5BOQ1K - GLUCOSAMINE
 

Glucosamine is an endogenous substance, a normal constituent of the polysaccharide chains of cartilage matrix and synovial fluid glucosaminoglycans. In vitro and in vivo studies have shown glucosamine stimulates the synthesis of physiological glycosaminoglycans and proteoglycans by chondrocytes and of hyaluronic acid by synoviocytes.

 
Read more about Glucosamine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 DOLENIO Film-coated tablets MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
M01AX05 Glucosamine M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AX Other antiinflammatory and antirheumatic agents, non-steroids
Discover more medicines within M01AX05

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1366028, 1368097, 1484355, 1484366, 1484377, 1484388, 1484399
FR Base de données publique des médicaments 60609568, 65144557
GB Medicines & Healthcare Products Regulatory Agency 170425
LT Valstybinė vaistų kontrolės tarnyba 1033363, 1038605, 1056818, 1056819, 1056820, 1056821, 1056822, 1056823, 1056824
MT Medicines Authority MA792/00101
NL Z-Index G-Standaard, PRK 97438
PL Rejestru Produktów Leczniczych 100213891

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