01 1AGEPHA Pharma US
02 2ALFA INTES (IND.TER.SPLENDORE)
03 1Abigo Medical AB
04 1Adcock Ingram
05 1Agepha Pharma Sro
06 2Alcon Inc
07 1Altaire Pharmaceuticals
08 4Bausch & Lomb Incorporated
09 1Ebb Medical
10 2Laboratorios Llorens Sa
11 2OmniVision
12 1SOLA BARNES HIND
13 1Santen Pharmaceutical
14 1Thea Pharma Sa
01 10Eye Drop
02 1Eye Drop Solution
03 1Eye drops, resolution
04 2OPD
05 3SOLUTION/DROPS;OPHTHALMIC
06 2Solution
07 2Blank
01 3Allowed
02 4Approved
03 2Authorized
04 2Cancelled
05 1DISCN
06 1Deregistered
07 2Originator
08 2RX
09 1Suspensed
10 3Blank
01 1ALTAFLUOR BENOX
02 1BENOXINATE HYDROCHLORIDE
03 2Benoxinato Cl
04 1Colirofta Double Anesthetic
05 1Colirofta Fluotest
06 1FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE
07 1Fluorescein Oxybuprocaine SDU Faure
08 1Fluress
09 1Minims Benoxinate Hydrochloride 0,4%
10 1Novesin
11 1Novesin Wander 0.4%
12 1Obupro
13 1Optax
14 2Oxibuprokain Bausch & Lomb
15 1Oxibuprokain Minims
16 1Oxybuproca?na Hydrochloride Agepha
17 1Oxybuprocaine SDU Faure
18 2Prescaina Llorens Eye Drops
01 2Italy
02 1Norway
03 2South Africa
04 5Spain
05 5Sweden
06 3Switzerland
07 3USA
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 : Originator
Registration Country : South Africa
Benoxinate (Oxybuprocaine) HCI
Brand Name : Novesin Wander 0.4%
Dosage Form : OPD
Dosage Strength : 50mg
Packaging : 3X1g/100ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Obupro
Dosage Form : Eye Drop
Dosage Strength : 4mg/ml
Packaging :
Approval Date : 25/04/2023
Application Number : 20220117000012
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Authorized
Registration Country : Spain
Oxybuprocaine Hydrochloride; Tetracaine Hydrochloride
Brand Name : Colirofta Double Anesthetic
Dosage Form : Solution
Dosage Strength : 1MG; 4 MG
Packaging :
Approval Date : 1957-01-01
Application Number : 27090
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Suspensed
Registration Country : Spain
Oxybuprocaine Hydrochloride; Sodium Fluorescein
Brand Name : Colirofta Fluotest
Dosage Form : Solution
Dosage Strength : 2.5MG; 4 MG
Packaging :
Approval Date : 1992-10-01
Application Number : 59104
Regulatory Info : Suspensed
Registration Country : Spain
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 : 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 :
Registration Country : Norway
Brand Name : Oxibuprokain Minims
Dosage Form : Eye drops, resolution
Dosage Strength : 4 mg/ml
Packaging : Endosebeholder
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Oxibuprokain Bausch & Lomb
Dosage Form : Eye Drop
Dosage Strength : 0.4% (4mg/ml)
Packaging :
Approval Date : 12/04/1984
Application Number : 19840412000049
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Minims Benoxinate Hydrochloride 0,4%
Dosage Form : OPD
Dosage Strength : 1mg/100ml
Packaging : 0.5X20g/100ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Oxibuprokain Bausch & Lomb
Dosage Form : Eye Drop
Dosage Strength : 0.4% (4mg/ml)
Packaging :
Approval Date : 03/12/2024
Application Number : 20240620000033
Regulatory Info : Approved
Registration Country : Sweden
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 : Allowed
Registration Country : Switzerland
Brand Name : Novesin
Dosage Form : Eye Drop
Dosage Strength : 0.004
Packaging :
Approval Date : 01/03/1971
Application Number : 36289
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 : DISCN
Registration Country : USA
Brand Name : BENOXINATE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.4%
Packaging :
Approval Date : 1982-01-01
Application Number : 84149
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Benoxinato Cl
Dosage Form :
Dosage Strength : Coll 10 Ml 0.4%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Benoxinato Cl
Dosage Form :
Dosage Strength : 100 Monod Coll 0.5 Ml 0.4%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Oxybuprocaine SDU Faure
Dosage Form : Eye Drop
Dosage Strength : 0.004
Packaging :
Approval Date : 26/04/1994
Application Number : 51523
Regulatory Info : Allowed
Registration Country : Switzerland
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Oxybuproca?na Hydrochloride Agepha
Dosage Form : Eye Drop Solution
Dosage Strength : 4MG
Packaging :
Approval Date : 2023-12-12
Application Number : 89170
Regulatory Info : Authorized
Registration Country : Spain
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Prescaina Llorens Eye Drops
Dosage Form : Eye Drop
Dosage Strength :
Packaging :
Approval Date : 1966-09-01
Application Number : 43319
Regulatory Info : Cancelled
Registration Country : Spain
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
