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European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eiyzey
Dosage Form : Injectable Solution In Vial
Dosage Strength : 40MG
Packaging :
Approval Date : 28-08-2025
Application Number : 1251963002
Regulatory Info : Authorized
Registration Country : Spain
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eiyzey
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 40MG
Packaging :
Approval Date : 28-08-2025
Application Number : 1251963001
Regulatory Info : Authorized
Registration Country : Spain
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Eiyzey
Dosage Form : Injection Solution
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Eiyzey
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Vgenfli
Dosage Form : Injection Solution
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Vgenfli
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
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 :
Registration Country : USA
Brand Name : ZALTRAP
Dosage Form : INJECTABLE; INJECTION
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number : 125418
Regulatory Info :
Registration Country : USA
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 : Zaltrap
Dosage Form : Concentrate For Solution For Perfusion
Dosage Strength : 100mg/4ml
Packaging :
Approval Date : 2013-03-20
Application Number : 62676
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 : Allowed
Registration Country : Switzerland
Brand Name : Zaltrap
Dosage Form : Concentrate For Solution For Infusion
Dosage Strength : 200mg/8ml
Packaging :
Approval Date : 2013-03-20
Application Number : 62676
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 : Authorized
Registration Country : Spain
Brand Name : Zaltrap
Dosage Form : Concentrate For Infusion Solution
Dosage Strength : 25MG
Packaging :
Approval Date : 22-02-2013
Application Number : 112814002
Regulatory Info : Authorized
Registration Country : Spain
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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
RLD :
TE Code :
Brand Name : ZALTRAP
Dosage Form : INJECTABLE; INJECTION
Dosage Strength : 4MG
Approval Date :
Application Number : 125418
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Brand Name : PAVBLU
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2 mg (0.05 mL of 40 mg/mL)
Approval Date :
Application Number : 761298
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : YESAFILI
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2MG(0.05ML,40MG/ML)
Approval Date :
Application Number : 761274
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EYDENZELT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2MG(0.05ML;40MG/ML)
Approval Date :
Application Number : 761377
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : AHZANTIVE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2MG(0.05ML OF 40MG/ML)
Approval Date :
Application Number : 761378
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EYLEA
Dosage Form : INJECTABLE; INJECTION
Dosage Strength : 40MG/ML
Approval Date :
Application Number : 125387
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EYLEA HD
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 8MG(0.07ML;114.3MG/ML)
Approval Date :
Application Number : 761355
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : OPUVIZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2MG(0.05ML,40MG/ML)
Approval Date :
Application Number : 761350
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : ENZEEVU
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2MG(0.05ML of 40MG/ML)
Approval Date :
Application Number : 761382
RX/OTC/DISCN :
RLD :
TE Code :

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European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eiyzey
Dosage Form : Injectable Solution In Vial
Dosage Strength : 40MG
Packaging :
Approval Date : 28-08-2025
Application Number : 1251963002
Regulatory Info : Authorized
Registration Country : Spain
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eiyzey
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 40MG
Packaging :
Approval Date : 28-08-2025
Application Number : 1251963001
Regulatory Info : Authorized
Registration Country : Spain
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Eiyzey
Dosage Form : Injection Solution
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Eiyzey
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Vgenfli
Dosage Form : Injection Solution
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Vgenfli
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 14-08-2025
Application Number : 2.02E+13
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 : Allowed
Registration Country : Switzerland
Brand Name : Zaltrap
Dosage Form : Concentrate For Solution For Infusion
Dosage Strength : 200mg/8ml
Packaging :
Approval Date : 2013-03-20
Application Number : 62676
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 : Authorized
Registration Country : Spain
Brand Name : Zaltrap
Dosage Form : Concentrate For Infusion Solution
Dosage Strength : 25MG
Packaging :
Approval Date : 22-02-2013
Application Number : 112814002
Regulatory Info : Authorized
Registration Country : Spain
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 : Zaltrap
Dosage Form : Concentrate For Infusion Solution
Dosage Strength : 25MG
Packaging :
Approval Date : 22-02-2013
Application Number : 112814001
Regulatory Info : Authorized
Registration Country : Spain
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 : Zaltrap
Dosage Form : Concentrate For Infusion Solution
Dosage Strength : 25MG
Packaging :
Approval Date : 22-02-2013
Application Number : 112814003
Regulatory Info : Authorized
Registration Country : Spain
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : SCHEDULE D
Registration Country : Canada
Brand Name : PAVBLU
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2550636
Regulatory Info : SCHEDULE D
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Brand Name : AFLIVU
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2554178
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : SCHEDULE D
Registration Country : Canada
Brand Name : AFLIVU
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2554194
Regulatory Info : SCHEDULE D
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Brand Name : EYLEA
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging : 278 MICROLITERS
Approval Date :
Application Number : 2415992
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Brand Name : EYLEA
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2505355
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Brand Name : EYLEA HD
Dosage Form : SOLUTION
Dosage Strength : 8MG/0.07ML
Packaging :
Approval Date :
Application Number : 2545004
Regulatory Info : PRESCRIPTION
Registration Country : Canada

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
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Regulatory Info : SCHEDULE D
Registration Country : Canada
Brand Name : EYLEA HD
Dosage Form : SOLUTION
Dosage Strength : 8MG/0.07ML
Packaging :
Approval Date :
Application Number : 2554798
Regulatory Info : SCHEDULE D
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
Brand Name : EYDENZELT
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2563037
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : SCHEDULE D
Registration Country : Canada
Brand Name : ENZEEVU
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2562510
Regulatory Info : SCHEDULE D
Registration Country : Canada

Regulatory Info : SCHEDULE D
Registration Country : Canada
Brand Name : YESAFILI
Dosage Form : SOLUTION
Dosage Strength : 2MG/0.05ML
Packaging :
Approval Date :
Application Number : 2535858
Regulatory Info : SCHEDULE D
Registration Country : Canada

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Patents & EXCLUSIVITIES
Patent Expiration Date : 2024-06-04
Date Granted : 2014-01-14
Brand Name : ZALTRAP
Patent Number : 2519875
Filing Date : 2004-06-04
Strength per Unit : 100 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2024-06-04
Date Granted : 2014-01-14
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07
Brand Name : ZALTRAP
Patent Number : 2376379
Filing Date : 2000-05-23
Strength per Unit : 100 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07
Patent Expiration Date : 2025-12-02
Date Granted : 2014-08-12
Brand Name : ZALTRAP
Patent Number : 2586735
Filing Date : 2005-12-02
Strength per Unit : 100 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2025-12-02
Date Granted : 2014-08-12
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07
Brand Name : ZALTRAP
Patent Number : 2376379
Filing Date : 2000-05-23
Strength per Unit : 200 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07
Patent Expiration Date : 2024-06-04
Date Granted : 2014-01-14
Brand Name : ZALTRAP
Patent Number : 2519875
Filing Date : 2004-06-04
Strength per Unit : 200 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2024-06-04
Date Granted : 2014-01-14
Patent Expiration Date : 2025-12-02
Date Granted : 2014-08-12
Brand Name : ZALTRAP
Patent Number : 2586735
Filing Date : 2005-12-02
Strength per Unit : 200 mg / vial
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVENOUS
Patent Expiration Date : 2025-12-02
Date Granted : 2014-08-12
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07
Brand Name : EYLEA
Patent Number : 2376379
Filing Date : 2000-05-23
Strength per Unit : 2mg / 0.05 mL
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVITREAL
Patent Expiration Date : 2020-05-23
Date Granted : 2007-08-07

Patent Expiration Date : 2027-06-14
Date Granted : 2015-03-17
Brand Name : EYLEA
Patent Number : 2654510
Filing Date : 2007-06-14
Strength per Unit : 2mg / 0.05 mL
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVITREAL
Patent Expiration Date : 2027-06-14
Date Granted : 2015-03-17

Patent Expiration Date : 1935-12-10
Date Granted : 2023-08-22
Brand Name : EYLEA HD
Patent Number : 2970315
Filing Date : 2015-12-10
Strength per Unit : 8mg / 0.07mL
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVITREAL
Patent Expiration Date : 1935-12-10
Date Granted : 2023-08-22

Patent Expiration Date : 1936-12-01
Date Granted : 2021-12-28
Brand Name : EYLEA HD
Patent Number : 3007276
Filing Date : 2016-12-01
Strength per Unit : 8mg / 0.07mL
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : INTRAVITREAL
Patent Expiration Date : 1936-12-01
Date Granted : 2021-12-28

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE