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01 2Sanofi Malta Limited

02 2Sanofi-Aventis Ab

03 1Acino Pharma Ag

04 1Cherubino Limited

05 2Cps Cito Pharma Services Gmbh

06 2Ebb Medical Ab

07 2Karo Pharma Ab

08 1Llorens Laboratories Sl

09 1Meda Ab

10 2Medius Ag

11 1Reig Jofre Laboratory, Sa

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Deregistered

Registration Country : Sweden

Cinchocaine Hydrochloride; Esculin; Framycetin Sulfate; Hydrocortisone

Brand Name : Proctosedyl

Dosage Form : Rectal Ointment

Dosage Strength :

Packaging :

Approval Date : 29/05/1962

Application Number : 19620529000039

Regulatory Info : Deregistered

Registration Country : Sweden

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.

Regulatory Info : Deregistered

Registration Country : Sweden

Cinchocaine Hydrochloride; Esculin; Framycetin Sulfate; Hydrocortisone

Brand Name : Proctosedyl

Dosage Form : Suppository

Dosage Strength :

Packaging :

Approval Date : 29/05/1962

Application Number : 19620529000046

Regulatory Info : Deregistered

Registration Country : Sweden

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.

Regulatory Info : Withdrawn

Registration Country : Malta

Cinchocaine Hydrochloride; Hydrocortisone

Brand Name : Proctosedyl

Dosage Form : Ointment

Dosage Strength : 0.5%W/W; 0.5%W/W

Packaging :

Approval Date : 2005-09-28

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

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.

Regulatory Info : Withdrawn

Registration Country : Malta

Cinchocaine Hydrochloride; Hydrocortisone

Brand Name : Proctosedyl

Dosage Form : Suppository

Dosage Strength : 5MG; 5MG

Packaging :

Approval Date : 2005-09-28

Application Number :

Regulatory Info : Withdrawn

Registration Country : Malta

Sanofi Company Banner

05

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Dequalinium Chloride; Cinchocaine Hydrochloride

Brand Name : Decatylen neo

Dosage Form : Lozenge

Dosage Strength :

Packaging :

Approval Date : 19/12/1988

Application Number : 50018

Regulatory Info : Allowed

Registration Country : Switzerland

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06

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Cinchocaine Hydrochloride; Prednisolone Caproate

Brand Name : Scheriproct

Dosage Form : Rectal Ointment

Dosage Strength : 0.19%;0.5%

Packaging :

Approval Date : 26/04/2024

Application Number : 20240116000011

Regulatory Info : Approved

Registration Country : Sweden

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07

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Cinchocaine Hydrochloride; Prednisolone Caproate

Brand Name : Scheriproct

Dosage Form : Rectal Ointment

Dosage Strength : 0.19%;0.5%

Packaging :

Approval Date : 21/02/2025

Application Number : 20241212000080

Regulatory Info : Approved

Registration Country : Sweden

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08

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Cinchocaine Hydrochloride; Prednisolone Caproate

Brand Name : Scheriproct

Dosage Form : Rectal Ointment

Dosage Strength : 0.19%;0.5%

Packaging :

Approval Date : 29/07/1965

Application Number : 19650729000010

Regulatory Info : Approved

Registration Country : Sweden

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09

CPhI India
Not Confirmed
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CPhI India
Not Confirmed

Cinchocaine Hydrochloride; Prednisolone Caproate

Brand Name : Scheriproct

Dosage Form : Suppository

Dosage Strength : 1.3mg/1mg

Packaging :

Approval Date : 29/07/1965

Application Number : 19650729000027

Regulatory Info : Approved

Registration Country : Sweden

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10

Meda Ab

Country
CPhI India
Not Confirmed
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Meda Ab

Country
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CPhI India
Not Confirmed

Cinocaine

Brand Name : Cincain

Dosage Form : Eye Ointment

Dosage Strength : 0.50%

Packaging :

Approval Date : 24/01/1975

Application Number : 19750124000063

Regulatory Info : Deregistered

Registration Country : Sweden

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