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01 4SANOFI-AVENTIS CANADA INC

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2024 ACI Convention
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Schedule D

Registration Country : Canada

RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN

Brand Name : ALPROLIX

Dosage Form : KIT

Dosage Strength : 500UNIT/VIAL

Packaging :

Approval Date :

Application Number : 2422913

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

02

arrow
2024 ACI Convention
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Schedule D

Registration Country : Canada

RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN

Brand Name : ALPROLIX

Dosage Form : KIT

Dosage Strength : 1000UNIT/VIAL

Packaging :

Approval Date :

Application Number : 2422921

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

03

arrow
2024 ACI Convention
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Schedule D

Registration Country : Canada

RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN

Brand Name : ALPROLIX

Dosage Form : KIT

Dosage Strength : 2000UNIT/VIAL

Packaging :

Approval Date :

Application Number : 2422948

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner

04

arrow
2024 ACI Convention
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Schedule D

Registration Country : Canada

RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN

Brand Name : ALPROLIX

Dosage Form : KIT

Dosage Strength : 3000UNIT/VIAL

Packaging :

Approval Date :

Application Number : 2422956

Regulatory Info : Schedule D

Registration Country : Canada

Sanofi Company Banner