Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 1GENZYME EUROPE B.V.
02 2Sanofi Bv
03 1Sanofi-Aventis (Switzerland) Sa
04 1Accord Healthcare S.L.U.
05 2Accord Healthcare Slu
06 1Auxilia Pharma Oü
07 1Eugia Pharma (Malta) Limited
08 1Glenmark Arzneimittel Gmbh
09 1Orifarm AS
10 2Seacross Pharma (Europe) Limited
11 1Seacross Pharma (Europe) Ltd.
12 1Stada Sl Laboratory
13 1Tarbis Farma Sl
14 1Teva GmbH
15 1Teva Gmbh
16 1Tillomed Spain Laboratories Sl
17 1Viatris Limited
18 1Vivanta Generics Sro
19 1Vivanta Generics sro
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01 1Jm 3100
02 1Many People
03 20Plerixafor
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01 15Injectable Solution
02 1Plerixafor 24Mg 1,2Ml 1 Unit Parenteral Use
03 6Solution For Injection
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01 2Estonia
02 1Italy
03 4Norway
04 8Spain
05 6Sweden
06 1Switzerland
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01 5Mozobil
02 1Plerazafor Accord
03 2Plerixafor Accord
04 1Plerixafor Auxilia
05 1Plerixafor Eugia
06 1Plerixafor Glenmark
07 3Plerixafor Seacross
08 1Plerixafor Stada
09 1Plerixafor Tarbis
10 2Plerixafor Teva
11 1Plerixafor Tillomed
12 1Plerixafor Viatris
13 2Plerixafor Vivanta
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Italy
Brand Name : Mozobil
Dosage Form : Plerixafor 24Mg 1,2Ml 1 Unit Parenteral Use
Dosage Strength : 1 bottle SC 24 mg 20 mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Mozobil
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 15/08/2014
Application Number : 63139
Regulatory Info : Allowed
Registration Country : Switzerland
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Mozobil
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 31/07/2009
Application Number : 20080608000019
Regulatory Info : Approved
Registration Country : Sweden
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Mozobil
Dosage Form : Injectable Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 12-11-2009
Application Number : 9537001
Regulatory Info : Authorized
Registration Country : Spain
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Plerixafor Accord
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 16/12/2022
Application Number : 20211012000016
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Not Marketed
Registration Country : Norway
Brand Name : Mozobil
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Not Marketed
Registration Country : Norway

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Plerixafor Seacross
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 25/04/2023
Application Number : 20210809000017
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Plerixafor Teva
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 11/07/2023
Application Number : 20210826000014
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Plerixafor Viatris
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 08/12/2023
Application Number : 20221020000021
Regulatory Info : Approved
Registration Country : Sweden

Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Plerixafor Vivanta
Dosage Form : Injectable Solution
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 03/07/2023
Application Number : 20210806000034
Regulatory Info : Approved
Registration Country : Sweden

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