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01 3Baxter Ag

02 1Baxter Medical Ab

03 2CSL Behring GmbH

04 12Csl Behring Gmbh

05 2Octapharma (IP) SPRL

06 6Octapharma Ab

07 3Octapharma Pharmazeutika Produktionsges. Mbh

08 1P & D Pharmaceuticals Limited

09 2Prothya Biosolutions Netherlands Bv

10 1Zlb Behring Gmbh

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PharmaCompass

01

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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

BIO Partnering at JPM
Not Confirmed
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BIO Partnering at JPM
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
BIO Partnering at JPM
Not Confirmed
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Zlb Behring Gmbh

Country
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BIO Partnering at JPM
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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