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Synopsis

Synopsis

ACTIVE PHARMA INGREDIENTS

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USDMF

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JDMF

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EU WC

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KDMF

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NDC API

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VMF

0INTERMEDIATES

REF. STANDARDS OR IMPURITIES

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EDQM

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USP

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FDF Dossiers

DRUG PRODUCT COMPOSITIONS

22RELATED EXCIPIENT COMPANIES

37EXCIPIENTS BY APPLICATIONS

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US Exclusivities

GLOBAL SALES INFORMATION

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Chemistry

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FDF Dossiers

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01

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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

Polpharma CB

02

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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

Polpharma CB

03

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

04

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

05

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

06

Polpharma

Poland
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

07

Sanofi

France
  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info :

Registration Country : USA

ZIV-AFLIBERCEPT

Brand Name : ZALTRAP

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 4MG

Packaging :

Approval Date :

Application Number : 125418

Regulatory Info :

Registration Country : USA

Sanofi Company Banner

08

Sanofi

France
  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Allowed

Registration Country : Switzerland

Aflibercept

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 Company Banner

09

Sanofi

France
  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Allowed

Registration Country : Switzerland

Aflibercept

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 Company Banner

10

Sanofi

France
  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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 Company Banner
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FDA Orange Book

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01

  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

RLD :

TE Code :

ZIV-AFLIBERCEPT

Brand Name : ZALTRAP

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 4MG

Approval Date :

Application Number : 125418

RX/OTC/DISCN :

RLD :

TE Code :

Sanofi Company Banner

02

AMGEN INC

U.S.A
RDD
Not Confirmed
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AMGEN INC

U.S.A
arrow
RDD
Not Confirmed

AFLIBERCEPT-AYYH

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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03

RDD
Not Confirmed
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RDD
Not Confirmed

AFLIBERCEPT-JBVF

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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04

CELLTRION INC

South Korea
RDD
Not Confirmed
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CELLTRION INC

South Korea
arrow
RDD
Not Confirmed

AFLIBERCEPT-BOAV

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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05

FORMYCON AG

Germany
RDD
Not Confirmed
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FORMYCON AG

Germany
arrow
RDD
Not Confirmed

AFLIBERCEPT-MRBB

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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06

RDD
Not Confirmed
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RDD
Not Confirmed

AFLIBERCEPT

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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07

RDD
Not Confirmed
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RDD
Not Confirmed

AFLIBERCEPT

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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08

RDD
Not Confirmed
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RDD
Not Confirmed

AFLIBERCEPT-YSZY

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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09

SANDOZ INC

Switzerland
RDD
Not Confirmed
arrow

SANDOZ INC

Switzerland
arrow
RDD
Not Confirmed

AFLIBERCEPT-ABZV

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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Europe

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01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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

Polpharma CB

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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

Polpharma CB

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Flag Poland
Digital Content Digital Content

Regulatory Info : Approved

Registration Country : Sweden

Aflibercept

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

Polpharma CB

07

  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Allowed

Registration Country : Switzerland

Aflibercept

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 Company Banner

08

  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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 Company Banner

09

  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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 Company Banner

10

  • fda
  • EDQM
  • WHO-GMP

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

Flag France
Digital Content Digital Content

Regulatory Info : Authorized

Registration Country : Spain

Aflibercept

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

Sanofi Company Banner
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Canada

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01

RDD
Not Confirmed
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RDD
Not Confirmed

AFLIBERCEPT

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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02

APOTEX INC

Canada
RDD
Not Confirmed
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APOTEX INC

Canada
arrow
RDD
Not Confirmed

AFLIBERCEPT

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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03

APOTEX INC

Canada
RDD
Not Confirmed
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APOTEX INC

Canada
arrow
RDD
Not Confirmed

AFLIBERCEPT

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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04

BAYER INC

Germany
RDD
Not Confirmed
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BAYER INC

Germany
arrow
RDD
Not Confirmed

AFLIBERCEPT

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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05

BAYER INC

Germany
RDD
Not Confirmed
arrow

BAYER INC

Germany
arrow
RDD
Not Confirmed

AFLIBERCEPT

Brand Name : EYLEA

Dosage Form : SOLUTION

Dosage Strength : 2MG/0.05ML

Packaging :

Approval Date :

Application Number : 2505355

Regulatory Info : PRESCRIPTION

Registration Country : Canada

blank

06

BAYER INC

Germany
RDD
Not Confirmed
arrow

BAYER INC

Germany
arrow
RDD
Not Confirmed

AFLIBERCEPT

Brand Name : EYLEA HD

Dosage Form : SOLUTION

Dosage Strength : 8MG/0.07ML

Packaging :

Approval Date :

Application Number : 2545004

Regulatory Info : PRESCRIPTION

Registration Country : Canada

blank

07

BAYER INC

Germany
RDD
Not Confirmed
arrow

BAYER INC

Germany
arrow
RDD
Not Confirmed

AFLIBERCEPT

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

blank

08

CELLTRION INC.

South Korea
RDD
Not Confirmed
arrow

CELLTRION INC.

South Korea
arrow
RDD
Not Confirmed

AFLIBERCEPT

Brand Name : EYDENZELT

Dosage Form : SOLUTION

Dosage Strength : 2MG/0.05ML

Packaging :

Approval Date :

Application Number : 2563037

Regulatory Info : PRESCRIPTION

Registration Country : Canada

blank

09

RDD
Not Confirmed
arrow
arrow
RDD
Not Confirmed

AFLIBERCEPT

Brand Name : ENZEEVU

Dosage Form : SOLUTION

Dosage Strength : 2MG/0.05ML

Packaging :

Approval Date :

Application Number : 2562510

Regulatory Info : SCHEDULE D

Registration Country : Canada

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10

BIOSIMILAR COLLABORATIONS IRELAND LIMITE...

Country
RDD
Not Confirmed
arrow

BIOSIMILAR COLLABORATIONS IRELAND LIMITE...

Country
arrow
RDD
Not Confirmed

AFLIBERCEPT

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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A company that specialises in the supply of various medical equipment such as MRI scanners, CT scanners, ultrasound machines, dialysis consumables is looking for suppliers of Various Finished Formulations: 1. Aflibercept 100 mg/4 ml (5 Units) & 200 mg/8 ml (5 Units) Vials 2. Bevacizumab 100 mg/4 ml (15 Units) & 400 mg/16 ml (15 Units) Vials 3. Bimatoprost 0.01% (1,000 Units), 0.3 mg/mL (1,000 Units) Ophthalmic Solution 4. Bimatoprost 0.3 mg/ml + Timolol 5 mg/ml (400 Units) Ophthalmic Solution 5. Brimonidine 0.15% w/v (1,000 Units) Ophthalmic Solution 6. Brimonidine 2 mg + Brinzolamide 10 mg (1000 Units) Ophthalmic Solution 7. Brimonidine Tartrate 2 mg + Timolol maleate 5 mg (3000 Units) Ophthalmic solution 8. Brinzolamide 1% w/v (1,000 Units) Ophthalmic Solution 9. Brinzolamide 10 mg + Timolol maleate 5 mg (1000 Units) Ophthalmic solution 10. Cyclopentolate Hydrochloride 0.5% (200 Units) & 1% (200 Units) Ophthalmic Solution 11. Epinastine Hydrochloride 0.5 mg/ ml (2,000 Units) Ophthalmic Solution 12. Fluorometholone 0.1 % w/v + Neomycin 0.35 % w/v (232 Units) Ophthalmic solution 13. Latanoprost 50 mcg (400 Units) + Timolol Maleate 6.8 mg (400 Units) Ophthalmic Solution 14. Latanoprost 50 mcg (2000 Units) Ophthalmic Solution 15. Levobunolol 0.5% (1,000 Units) Ophthalmic Solution 16. Moxifloxacin Hydrochloride 5.45 mg/ml (2,000 Units) Ophthalmic Solution 17. Nepafenac 1 mg (1,000 Units) & 3 mg (1,000 Units) Ophthalmic Solution 18. Ofloxacin 0.3% w/v (81 Units) Ophthalmic Solution 19. Olopatadine 1 mg/ml (2,000 Units) Ophthalmic Solution 20. Polyethylene Glycol 400 0.4% + Propylene Glycol 0.3% (1,000 Units) Ophthalmic Solution 21. Polyvinyl Alcohol 1.4% (5,000 Units) Ophthalmic Solution 22. Povidone 0.6% (5,000 Units) Ophthalmic Solution 23. Prednisolone Acetate (microfine suspension) 1% (1,000 Units) Ophthalmic Solution 24. Travoprost 40 mcg/ml + Timolol Maleate 5 mg/ml (400 Units) Ophthalmic Solution 25. Timolol 6.8 mg (400 Units) Ophthalmic Solution 26. Travoprost 0.004 % (2,000 Units) Ophthalmic Solution
15 Feb 2020

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15 Feb 2020

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15 Feb 2020

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Patents & EXCLUSIVITIES

Check the patents & exclusivity for this product

Health Canada Patents

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01

  • fda
  • EDQM
  • WHO-GMP

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

Patent Expiration Date : 2024-06-04

Date Granted : 2014-01-14

AFLIBERCEPT

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

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Patent Expiration Date : 2020-05-23

Date Granted : 2007-08-07

AFLIBERCEPT

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

Sanofi Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

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

Patent Expiration Date : 2025-12-02

Date Granted : 2014-08-12

AFLIBERCEPT

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

Sanofi Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

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

Patent Expiration Date : 2020-05-23

Date Granted : 2007-08-07

AFLIBERCEPT

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

Sanofi Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

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

Patent Expiration Date : 2024-06-04

Date Granted : 2014-01-14

AFLIBERCEPT

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

Sanofi Company Banner

06

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

Patent Expiration Date : 2025-12-02

Date Granted : 2014-08-12

AFLIBERCEPT

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

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Bayer Inc.

Germany
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AFLIBERCEPT

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

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Bayer Inc.

Germany
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Not Confirmed

AFLIBERCEPT

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

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09

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Bayer Inc.

Germany
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Not Confirmed

AFLIBERCEPT

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

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10

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RDD
Not Confirmed

Bayer Inc.

Germany
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RDD
Not Confirmed

AFLIBERCEPT

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

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