01 1Abigo Medical AB
02 4Alcon Inc
03 1Altaire Pharmaceuticals
04 1Aurolab
05 5Bausch & Lomb Incorporated
06 1Central Procurement & Supplies Unit
07 1Chauvin Phamaceuticals Limited
08 2Curatis
09 2Laboratorios Poen
10 1MONICO SpA
11 1OmniVision
12 1Polifarma
13 1Santen Pharmaceutical
14 1Serb
01 6Eye Drop
02 2Eye Drop Solution
03 1Fluorescein 20% 1G 5Ml 10 Units Parenteral Use
04 2INJ
05 1IV Injection Solution
06 1Injectable Solution
07 1Injection
08 1Injection fluid, resolution
09 2Ophthalmic Solution
10 2SOLUTION/DROPS;OPHTHALMIC
11 3Solution For Injection
12 1Strip
01 3Allowed
02 4Approved
03 4Authorised
04 1Deregistered
05 2Originator
06 2RX
07 1Withdrawn
08 6Blank
01 1ALTAFLUOR BENOX
02 1Anatera
03 1FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE
04 1Fluocyne
05 1Fluorescein
06 1Fluorescein SDU Faure
07 1Fluorescein Oxybuprocaine SDU Faure
08 1Fluorescein Sodium Bausch & Lomb
09 1Fluoresceine Faure
10 1Fluorescite
11 1Fluorescite 10%
12 1Fluorescite 25% 5Ml
13 1Fluorets
14 1Flures
15 1Fluress
16 1Fotoptic
17 1Lidokain-Fluorescein Bausch & Lomb
18 1Minims Fluorescein
19 1Minims Lidocaine & Fluorescein
20 1Optax
21 1Sodium Fluorescein
22 2Blank
01 2Argentina
02 1India
03 1Italy
04 5Malta
05 1Norway
06 2South Africa
07 5Sweden
08 3Switzerland
09 1Turkey
10 2USA
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 : RX
Registration Country : USA
BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
Brand Name : ALTAFLUOR BENOX
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.4%;0.25%
Packaging :
Approval Date : 2017-12-14
Application Number : 208582
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Flures
Dosage Form : Injection
Dosage Strength : 20%/W/V
Packaging : 10 Ampules / Box
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
Brand Name : FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.4%;0.3%
Packaging :
Approval Date : 2020-03-09
Application Number : 211039
Regulatory Info : RX
Registration Country : USA
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 : Authorised
Registration Country : Malta
Brand Name : Minims Fluorescein
Dosage Form : Eye Drop Solution
Dosage Strength : 1%W/V
Packaging :
Approval Date : 2024-09-04
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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 :
Registration Country : Argentina
Brand Name :
Dosage Form : Ophthalmic Solution
Dosage Strength : 0.25%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Argentina
Regulatory Info :
Registration Country : Argentina
Brand Name : Fotoptic
Dosage Form : Ophthalmic Solution
Dosage Strength : 0.5%; 0.25%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Argentina
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 :
Registration Country : Turkey
Brand Name :
Dosage Form : IV Injection Solution
Dosage Strength : 500MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
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 : Authorised
Registration Country : Malta
Brand Name : Fluocyne
Dosage Form : Solution For Injection
Dosage Strength : 100ML
Packaging :
Approval Date : 2025-01-20
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Fluorets
Dosage Form : Strip
Dosage Strength : 1MG
Packaging :
Approval Date : 2005-10-04
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Fluorescein
Dosage Form : Solution For Injection
Dosage Strength : 100MG/ML
Packaging :
Approval Date : 2024-12-05
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
