INDUCTOS

This brand name is authorized in Austria, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Poland, United Kingdom

Active ingredients

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

1 Dibotermin alfa
UNII T472P45MG6 - DIBOTERMIN ALFA

Dibotermin alfa is an osteoinductive protein that results in the induction of new bone tissue at the site of implantation. Dibotermin alfa binds to receptors on the surface of mesenchymal cells and causes cells to differentiate into cartilage- and bone-forming cells. The differentiated cells form trabecular bone as the matrix is degraded, with vascular invasion evident at the same time.

Read about Dibotermin alfa

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
INDUCTOS Powder, solvent and matrix for implantation matrix European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
M05BC01 Dibotermin alfa M Musculo-skeletal system → M05 Drugs for treatment of bone diseases → M05B Drugs affecting bone structure and mineralization → M05BC Bone morphogenetic proteins
Discover more medicines within M05BC01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1212376, 1703360
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 02226001
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 181720
Country: FR Base de données publique des médicaments Identifier(s): 60897889
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 385296, 89931
Country: IT Agenzia del Farmaco Identifier(s): 035913019
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1028450, 1078251
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100219451

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