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01 1SANOFI-AVENTIS CANADA INC

02 1JAMP PHARMA CORPORATION

03 2ODAN LABORATORIES LTD

04 2PENDOPHARM DIVISION OF PHARMASCIENCE INC

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PharmaCompass

01

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Fi Europe 2024
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 : Prescription

Registration Country : Canada

SODIUM POLYSTYRENE SULFONATE

Brand Name : KAYEXALATE

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 1G/G

Packaging : 454 GM

Approval Date :

Application Number : 2026961

Regulatory Info : Prescription

Registration Country : Canada

Sanofi Company Banner

02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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SODIUM POLYSTYRENE SULFONATE

Brand Name : JAMP SODIUM POLYSTYRENE SULFONATE

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 1G/G

Packaging :

Approval Date :

Application Number : 2497557

Regulatory Info : Prescription

Registration Country : Canada

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03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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SODIUM POLYSTYRENE SULFONATE

Brand Name : ODAN-SODIUM POLYSTYRENE SULFONATE

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 1G/G

Packaging : 454 G

Approval Date :

Application Number : 2473941

Regulatory Info : Prescription

Registration Country : Canada

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04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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SODIUM POLYSTYRENE SULFONATE

Brand Name : ODAN-SODIUM POLYSTYRENE SULFONATE

Dosage Form : SUSPENSION

Dosage Strength : 250MG/ML

Packaging : 60ML/500ML

Approval Date :

Application Number : 2473968

Regulatory Info : Prescription

Registration Country : Canada

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05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
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SODIUM POLYSTYRENE SULFONATE

Brand Name : SOLYSTAT

Dosage Form : POWDER FOR SUSPENSION

Dosage Strength : 1G/G

Packaging : 454G

Approval Date :

Application Number : 755338

Regulatory Info : Prescription

Registration Country : Canada

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06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

SODIUM POLYSTYRENE SULFONATE

Brand Name : SOLYSTAT

Dosage Form : SUSPENSION

Dosage Strength : 250MG/ML

Packaging : 60ML/500ML

Approval Date :

Application Number : 769541

Regulatory Info : Prescription

Registration Country : Canada

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