VERASEAL

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

Active ingredients

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

1 Human fibrinogen
UNII N94833051K - FIBRINOGEN HUMAN

Human fibrinogen (coagulation factor I), in the presence of thrombin, activated coagulation factor XIII (F XIIIa) and calcium ions is converted into a stable and elastic three-dimensional fibrin haemostatic clot. The administration of human fibrinogen concentrate provides an increase in plasma fibrinogen level and can temporarily correct the coagulation defect of patients with fibrinogen deficiency.

Read about Human fibrinogen
2 Thrombin
UNII 6K15ABL77G - HUMAN THROMBIN
Read about Thrombin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
VERASEAL Solutions for sealant 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
B02BC Local hemostatics B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics
Discover more medicines within B02BC

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): 1756975, 1756986, 1756997, 1757000
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 390133, 595671
Country: FR Base de données publique des médicaments Identifier(s): 67065507
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 390263, 390267, 390270
Country: IT Agenzia del Farmaco Identifier(s): 045788015, 045788027, 045788039, 045788041
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1084494, 1084495, 1084496, 1084497
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100400021

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