EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 3Sanofi
03 1Aldo-Union
04 1Boehringer Ingelheim GmbH
05 1Central Procurement & Supplies Unit
06 1Cherubino Limited
07 2DECHRA VETERINARY PRODUCTS AS
08 1Galenicum
09 1Laboratorio De Aplicaciones Farmacodinamicas Sa
10 2Pharmaco
11 1Rottapharm Biotech
01 2Cream
02 2Ear Drop
03 1Ear Drop In Suspension
04 2Ear Drops Suspension
05 2Ear Drops, Solution, Eye Drops, Solution
06 1Eye/Ear Drops
07 1Intramammary Suspension
08 2Ointment
09 1Rectal Ointment
10 1Suppository
01 1Authorised
02 2Authorized
03 2Cancelled
04 3Deregistered
05 1Invalid
06 1Marketed
07 1Not Marketed
08 1Prescription
09 1Withdrawn
10 2Blank
01 1Abicrem
02 1Aldoderma
03 1Benestermycin Vet.
04 2Canaural knows
05 1Nesfare Cream
06 1Otodex
07 1Otomidrin
08 3Proctosedyl
09 2Sofradex
10 2Sofradex Ear/Eye
01 2Australia
02 1Denmark
03 3Malta
04 2Norway
05 4Spain
06 3Sweden
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Regulatory Info : Deregistered
Registration Country : Sweden
Dexamethasone Sodium Metasulfobenzoate; Framycetin Sulfate; Gramicidin
Brand Name : Sofradex
Dosage Form : Eye/Ear Drops
Dosage Strength :
Packaging :
Approval Date : 09/12/1963
Application Number : 19631209000027
Regulatory Info : Deregistered
Registration Country : Sweden
Sanofi 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 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 is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Withdrawn
Registration Country : Malta
Framycetin Sulfate; Dexamethasone; Gramicidin
Brand Name : Sofradex Ear/Eye
Dosage Form : Ear Drops, Solution, Eye Drops, Solution
Dosage Strength : 0.5%W/V; 0.05%W/V; 0.005%W/V
Packaging :
Approval Date : 2005-09-28
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Authorized
Registration Country : Spain
Triamcinolone Acetonide; Framycetin Sulfate
Brand Name : Aldoderma
Dosage Form : Ointment
Dosage Strength : 1MG; 3.5 MG
Packaging :
Approval Date : 01-03-1966
Application Number : 42725
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Prescription
Registration Country : Denmark
Benethamine Penicillin; Benethamine Penicillin; Framycetin Sulphate; Penethamate Hydroiodide
Brand Name : Benestermycin Vet.
Dosage Form : Intramammary Suspension
Dosage Strength :
Packaging :
Approval Date : 28-06-1974
Application Number : 28100578370
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info : Not Marketed
Registration Country : Norway
Diethanolamine fusidate; Framycetin sulfate; Nystatin; Prednisolone
Brand Name : Canaural knows
Dosage Form : Ear Drops Suspension
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info : Not Marketed
Registration Country : Norway
Regulatory Info : Marketed
Registration Country : Norway
Diethanolamine fusidate; Framycetin sulfate; Nystatin; Prednisolone
Brand Name : Canaural knows
Dosage Form : Ear Drops Suspension
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Authorized
Registration Country : Spain
Fluocinolone Acetonide; Framycetin Sulfate
Brand Name : Abicrem
Dosage Form : Cream
Dosage Strength : 0.25MG; 5 MG
Packaging :
Approval Date : 01-02-1972
Application Number : 49840
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info :
Registration Country : Australia
framycetin sulfate + gramicidin + dexamethasone
Brand Name : Otodex
Dosage Form : Ear Drop
Dosage Strength : 0.5%
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
framycetin sulfate + gramicidin + dexamethasone
Brand Name : Sofradex
Dosage Form : Ear Drop
Dosage Strength : 0.5%
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info : Cancelled
Registration Country : Spain
Triamcinolone Acetonide; Framycetin Sulfate; Centella Asiatica Exto
Brand Name : Nesfare Cream
Dosage Form : Cream
Dosage Strength :
Packaging :
Approval Date : 01-03-1973
Application Number : 50539
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Invalid
Registration Country : Malta
Framycetin Sulfate; Gramicidin; Dexamethasone
Brand Name : Sofradex Ear/Eye
Dosage Form : Ear Drops, Solution, Eye Drops, Solution
Dosage Strength : 5MG/ML; 0.05MG/ML; 0.05MG/ML
Packaging :
Approval Date : 2020-12-15
Application Number :
Regulatory Info : Invalid
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorised
Registration Country : Malta
Framycetin Sulfate; Hydrocortisone; Aesculin; Cinchocaine Hydrochloride
Brand Name : Proctosedyl
Dosage Form : Ointment
Dosage Strength : 10MG/G; 5MG/G; 10MG/G; 5MG/G
Packaging :
Approval Date : 2025-05-02
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Cancelled
Registration Country : Spain
Fluocinolone Acetonide; Framycetin Sulfate; Lidocaine Hydrochloride
Brand Name : Otomidrin
Dosage Form : Ear Drop In Suspension
Dosage Strength : 8MG; 0.25MG; 20 MG
Packaging :
Approval Date : 01-06-1981
Application Number : 55286
Regulatory Info : Cancelled
Registration Country : Spain
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
