
Reset all filters
01 1Abigo Medical Ab
02 2Alcon Nordic A/S
03 2Bausch & Lomb Ireland Limited
04 2Curatis Ag
05 1MONICO SpA
06 1Omnivision Ag
07 1Santen Oy
Reset all filters
01 2Fluorescein
02 2Fluorescein Sodium
03 1Fluorescein Sodium; Lidocaine Hydrochloride (Anhydrous)
04 3Fluorescein Sodium; Oxybuprocaine Hydrochloride
05 2Sodium Fluorescein
Reset all filters
01 6Eye Drop
02 1Fluorescein 20% 1G 5Ml 10 Units Parenteral Use
03 1Injectable Solution
04 1Injection fluid, resolution
05 1Solution For Injection
Reset all filters
01 1Italy
02 1Norway
03 5Sweden
04 3Switzerland
Reset all filters
01 1Anatera
02 1Fluorescein SDU Faure
03 1Fluorescein Oxybuprocaine SDU Faure
04 1Fluorescein Sodium Bausch & Lomb
05 1Fluoresceine Faure
06 1Fluorescite
07 1Fluress
08 1Lidokain-Fluorescein Bausch & Lomb
09 1Optax
10 1Sodium Fluorescein
Regulatory Info : Deregistered
Registration Country : Sweden
Fluorescein Sodium; Oxybuprocaine Hydrochloride
Brand Name : Fluress
Dosage Form : Eye Drop
Dosage Strength : 2.5mg/ml;4mg/ml
Packaging :
Approval Date : 30/12/1993
Application Number : 19931230000103
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info :
Registration Country : Norway
Brand Name : Anatera
Dosage Form : Injection fluid, resolution
Dosage Strength : 100 mg/ml
Packaging : Hood glass
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Fluorescite
Dosage Form : Injectable Solution
Dosage Strength : 100mg/ml
Packaging :
Approval Date : 15/06/2007
Application Number : 20060919000014
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Fluorescein Sodium Bausch & Lomb
Dosage Form : Eye Drop
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 05/02/1982
Application Number : 19820205000081
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Fluorescein Sodium; Lidocaine Hydrochloride (Anhydrous)
Brand Name : Lidokain-Fluorescein Bausch & Lomb
Dosage Form : Eye Drop
Dosage Strength :
Packaging :
Approval Date : 07/09/1984
Application Number : 19840907000011
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Fluorescein SDU Faure
Dosage Form : Eye Drop
Dosage Strength : 0.005
Packaging :
Approval Date : 23/10/1987
Application Number : 46996
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Fluoresceine Faure
Dosage Form : Solution For Injection
Dosage Strength : 500mg/5ml
Packaging :
Approval Date : 10/08/1999
Application Number : 54604
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Fluorescein Sodium; Oxybuprocaine Hydrochloride
Brand Name : Fluorescein Oxybuprocaine SDU Faure
Dosage Form : Eye Drop
Dosage Strength :
Packaging :
Approval Date : 11/01/1999
Application Number : 54756
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Fluorescein Sodium; Oxybuprocaine Hydrochloride
Brand Name : Optax
Dosage Form : Eye Drop
Dosage Strength : 1.25mg/ml;3mg/ml
Packaging :
Approval Date : 26/04/2018
Application Number : 20170328000021
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : Sodium Fluorescein
Dosage Form : Fluorescein 20% 1G 5Ml 10 Units Parenteral Use
Dosage Strength : 10 VIALS EV
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF