01 1Abigo Medical AB
02 4Alcon Inc
03 1Altaire Pharmaceuticals
04 1Aurolab
05 3Bausch & Lomb Incorporated
06 2Curatis
07 2Laboratorios Poen
08 1MONICO SpA
09 1OmniVision
10 1Polifarma
11 1Santen Pharmaceutical
01 6Eye Drop
02 1Fluorescein 20% 1G 5Ml 10 Units Parenteral Use
03 2INJ
04 1IV Injection Solution
05 1Injectable Solution
06 1Injection
07 1Injection fluid, resolution
08 2Ophthalmic Solution
09 2SOLUTION/DROPS;OPHTHALMIC
10 1Solution For Injection
01 3Allowed
02 4Approved
03 1Deregistered
04 2Originator
05 2RX
06 6Blank
01 1ALTAFLUOR BENOX
02 1Anatera
03 1FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE
04 1Fluorescein SDU Faure
05 1Fluorescein Oxybuprocaine SDU Faure
06 1Fluorescein Sodium Bausch & Lomb
07 1Fluoresceine Faure
08 1Fluorescite
09 1Fluorescite 10%
10 1Fluorescite 25% 5Ml
11 1Flures
12 1Fluress
13 1Fotoptic
14 1Lidokain-Fluorescein Bausch & Lomb
15 1Optax
16 1Sodium Fluorescein
17 2Blank
01 2Argentina
02 1India
03 1Italy
04 1Norway
05 2South Africa
06 5Sweden
07 3Switzerland
08 1Turkey
09 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 : Originator
Registration Country : South Africa
Brand Name : Fluorescite 10%
Dosage Form : INJ
Dosage Strength : 500mg/5ml
Packaging : 5X12mg/5ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Fluorescite 25% 5Ml
Dosage Form : INJ
Dosage Strength : 25%
Packaging : 12X1%
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
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 : 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 :
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
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