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01 2Baxalta Innovations GmbH

02 1Baxalta Innovations Gmbh

03 3Baxter Ag

04 1Baxter Medical Ab

05 5Bayer Ag

06 5CSL Behring GmbH

07 19Csl Behring Gmbh

08 7Octapharma (2)

09 2Octapharma (IP) SPRL

10 8Octapharma Ab

11 3Octapharma Pharmazeutika Produktionsges. Mbh

12 1Orifarm AS

13 1P & D Pharmaceuticals Limited

14 2Prothya Biosolutions Netherlands Bv

15 1Zlb Behring Gmbh

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PharmaCompass

01

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Aprotinin Bovine Synthetic; Human Fibrinogen; Calcium Chloride Dihydrate; Human Coagulation Factor XIII; Human Thrombin

Brand Name : Tisseel

Dosage Form : Solution

Dosage Strength :

Packaging :

Approval Date : 29/01/2010

Application Number : 20070210000019

Regulatory Info : Approved

Registration Country : Sweden

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02

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Aprotinin Bovine; Human Fibrinogen; Calcium Chloride Dihydrate; Human Coagulation Factor XIII; Human Thrombin

Brand Name : Tisseel

Dosage Form : Solution

Dosage Strength :

Packaging :

Approval Date : 26/02/2010

Application Number : 20070210000026

Regulatory Info : Deregistered

Registration Country : Sweden

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03

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Aprotinin Bovine; Human Fibrinogen; Human Fibronectin; Calcium Chloride Dihydrate; Human Coagulation Factor XIII; Human Plasminogen; Human Thrombin

Brand Name : Tisseel Kit

Dosage Form : Solution

Dosage Strength :

Packaging :

Approval Date : 19/01/1995

Application Number : 19950119000027

Regulatory Info : Deregistered

Registration Country : Sweden

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04

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Aprotinin Bovine; Human Fibrinogen; Human Fibronectin; Calcium Chloride Dihydrate; Human Coagulation Factor XIII; Human Plasminogen; Human Thrombin

Brand Name : Tisseel Duo Quick

Dosage Form : Solution

Dosage Strength :

Packaging :

Approval Date : 19/01/1995

Application Number : 19950119000010

Regulatory Info : Deregistered

Registration Country : Sweden

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05

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Coagulation Factor VIII Human; Von Willebrand Factor Human

Brand Name : Haemate

Dosage Form : Injection/Infusion Solution

Dosage Strength : 1000IUFVIII/2400IUVWF

Packaging :

Approval Date : 12/06/1987

Application Number : 19870612000136

Regulatory Info : Approved

Registration Country : Sweden

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06

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Coagulation Factor VIII Human; Von Willebrand Factor Human

Brand Name : Haemate

Dosage Form : Injection/Infusion Solution

Dosage Strength : 500IUFVIII/1200IUVWF

Packaging :

Approval Date : 12/06/1987

Application Number : 19870612000051

Regulatory Info : Approved

Registration Country : Sweden

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07

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Coagulation Factor VIII Human; Von Willebrand Factor Human

Brand Name : Voncento

Dosage Form : Injection/Infusion Solution

Dosage Strength : 1000IUFVIII/2400IUVWF

Packaging :

Approval Date : 12/08/2013

Application Number : 20120121000056

Regulatory Info : Approved

Registration Country : Sweden

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08

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Coagulation Factor VIII Human; Von Willebrand Factor Human

Brand Name : Voncento

Dosage Form : Injection/Infusion Solution

Dosage Strength : 250IEFVIII/600IEVWF

Packaging :

Approval Date : 12/08/2013

Application Number : 20120121000025

Regulatory Info : Approved

Registration Country : Sweden

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09

PharmaSynergy
Not Confirmed
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PharmaSynergy
Not Confirmed

Coagulation Factor VIII Human; Von Willebrand Factor Human

Brand Name : Voncento

Dosage Form : Injection/Infusion Solution

Dosage Strength : 10ml

Packaging :

Approval Date : 12/08/2013

Application Number : 20120121000032

Regulatory Info : Approved

Registration Country : Sweden

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10

Zlb Behring Gmbh

Country
PharmaSynergy
Not Confirmed
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Zlb Behring Gmbh

Country
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PharmaSynergy
Not Confirmed

Aprotinin Bovine; Human Fibrinogen; Calcium Chloride Dihydrate; Human Coagulation Factor XIII; Human Thrombin

Brand Name : Beriplast P Combi-Set

Dosage Form : Solution

Dosage Strength :

Packaging :

Approval Date : 10/08/2001

Application Number : 20010810000125

Regulatory Info : Deregistered

Registration Country : Sweden

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