FULLBONE D3

This brand name is authorized in Turkey.

Active ingredients

The drug FULLBONE D3 contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 04NQ160FRU - STRONTIUM RANELATE
 

In vitro, strontium ranelate increases bone formation in bone tissue culture as well as osteoblast precursor replication and collagen synthesis in bone cell culture and reduces bone resorption by decreasing osteoclast differentiation and resorbing activity. This results in a rebalance of bone turnover in favour of bone formation.

 
Read more about Strontium ranelate
2
UNII 1C6V77QF41 - CHOLECALCIFEROL
 

In its biologically active form vitamin D3 stimulates intestinal calcium absorption, incorporation of calcium into the osteoid, and release of calcium from bone tissue. In the small intestine it promotes rapid and delayed calcium uptake. The passive and active transport of phosphate is also stimulated.

 
Read more about Vitamin D3

Medicine classification

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

ATC Group Classification
A11CC05 Colecalciferol A Alimentary tract and metabolism → A11 Vitamins → A11C Vitamin A and D, incl. combinations of the two → A11CC Vitamin D and analogues
Discover more medicines within A11CC05
M05BX03 Strontium ranelate M Musculo-skeletal system → M05 Drugs for treatment of bone diseases → M05B Drugs affecting bone structure and mineralization → M05BX Other drugs affecting bone structure and mineralization
Discover more medicines within M05BX03

Authorization and marketing

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

Country Identification scheme Identifier(s)
TR İlaç ve Tıbbi Cihaz Kurumu 8699976021007, 8699976021205

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