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    Benoxinate Hydrochloride

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    01

    AGEPHA Pharma US

    U.S.A
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    Regulatory Info : Prescription

    Registration Country : Estonia

    Oxybuprocaine

    Brand Name : Novain

    Dosage Form : Ophthalmic Solution

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    Alcon Inc

    U.S.A
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    Regulatory Info : Authorized

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    Oxybuprocaine Hydrochloride; Tetracaine Hydrochloride

    Brand Name : Colirofta Double Anesthetic

    Dosage Form : Solution

    Dosage Strength : 1MG; 4 MG

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    Approval Date : 01-01-1957

    Application Number : 27090

    Regulatory Info : Authorized

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    Alcon Inc

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    Regulatory Info : Suspended

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    Oxybuprocaine Hydrochloride; Sodium Fluorescein

    Brand Name : Colirofta Fluotest

    Dosage Form : Solution

    Dosage Strength : 2.5MG; 4 MG

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    Approval Date : 01-10-1992

    Application Number : 59104

    Regulatory Info : Suspended

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    Altaire Pharmaceuticals

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    Regulatory Info : RX

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    BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM

    Brand Name : ALTAFLUOR BENOX

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 0.4%;0.25%

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    Approval Date : 2017-12-14

    Application Number : 208582

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    Bausch & Lomb Incorporated

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    BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM

    Brand Name : FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 0.4%;0.3%

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    Approval Date : 2020-03-09

    Application Number : 211039

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    Bausch & Lomb Incorporated

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    Regulatory Info : Authorised

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    Oxybuprocaine Hydrochloride

    Brand Name : Minims Oxybuprocaine Hydrochloride

    Dosage Form : Eye Drop Solution

    Dosage Strength : 0.4%W/V

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    Approval Date : 2005-10-04

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    Regulatory Info : Authorised

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    Bausch & Lomb Incorporated

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    Regulatory Info : Marketed

    Registration Country : Norway

    Oxybuprocaine hydrochloride

    Brand Name : Oxibuprocaine Minims

    Dosage Form : Eye Drops

    Dosage Strength : 4mg/ml

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    OmniVision

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    Regulatory Info : Allowed

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    Fluorescein Sodium; Oxybuprocaine Hydrochloride

    Brand Name : Fluorescein Oxybuprocaine SDU Faure

    Dosage Form : Eye Drop

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    Approval Date : 11/01/1999

    Application Number : 54756

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    OmniVision

    Switzerland
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    Regulatory Info : Allowed

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    Oxybuprocaine Hydrochloride

    Brand Name : Novesin

    Dosage Form : Eye Drop

    Dosage Strength : 0.004

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    Approval Date : 01/03/1971

    Application Number : 36289

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    10

    S.C. Rompharm Company SRL

    Romania
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    Regulatory Info :

    Registration Country : Moldova

    Oxybuprocaine

    Brand Name : Oftacain

    Dosage Form : Ophthalmic Solution

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    Approval Date : 26-12-2024

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    Regulatory Info :

    Registration Country : Moldova

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    Santen Pharmaceutical

    Japan
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    Regulatory Info : Marketed

    Registration Country : Norway

    Fluorescein sodium; Oxybuprocaine hydrochloride

    Brand Name : Combiflur

    Dosage Form : Eye Drops

    Dosage Strength : 1.25mg/ml; 3mg/ml

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    Regulatory Info : Marketed

    Registration Country : Norway

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    12

    SOLA BARNES HIND

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    Regulatory Info : DISCN

    Registration Country : USA

    BENOXINATE HYDROCHLORIDE

    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

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    ALFA INTES (IND.TER.SPLENDORE)

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    Regulatory Info :

    Registration Country : Italy

    Benoxinate

    Brand Name : Benoxinato Cl

    Dosage Form :

    Dosage Strength : Coll 10 Ml 0.4%

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    Regulatory Info :

    Registration Country : Italy

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    ALFA INTES (IND.TER.SPLENDORE)

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    Regulatory Info :

    Registration Country : Italy

    Benoxinate

    Brand Name : Benoxinato Cl

    Dosage Form :

    Dosage Strength : 100 Monod Coll 0.5 Ml 0.4%

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    Registration Country : Italy

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    Thea Pharma Sa

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Oxybuprocaine Hydrochloride

    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

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    Central Procurement & Supplies Unit

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    BioAsia
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    Regulatory Info : Invalid

    Registration Country : Malta

    Oxybuprocaine Hydrochloride

    Brand Name : Minims Oxybuprocaine Hydrochloride

    Dosage Form : Eye Drop Solution

    Dosage Strength : 0.4%W/V

    Packaging :

    Approval Date : 2020-02-24

    Application Number :

    Regulatory Info : Invalid

    Registration Country : Malta

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    Central Procurement & Supplies Unit

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    Regulatory Info : Authorised

    Registration Country : Malta

    Oxybuprocaine Hydrochloride

    Brand Name : Conjuncain Edo

    Dosage Form : Eye Drop Solution

    Dosage Strength : 4MG/ML

    Packaging :

    Approval Date : 2025-07-04

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    Regulatory Info : Authorised

    Registration Country : Malta

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    Agepha Pharma Sro

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    Regulatory Info : Authorized

    Registration Country : Spain

    Oxybuprocaine Hydrochloride

    Brand Name : Oxybuproca?na Hydrochloride Agepha

    Dosage Form : Eye Drop Solution

    Dosage Strength : 4MG

    Packaging :

    Approval Date : 12-12-2023

    Application Number : 89170

    Regulatory Info : Authorized

    Registration Country : Spain

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    Laboratorios Llorens Sa

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    Regulatory Info : Cancelled

    Registration Country : Spain

    Oxybuprocaine

    Brand Name : Prescaina Llorens Eye Drops

    Dosage Form : Eye Drop

    Dosage Strength :

    Packaging :

    Approval Date : 01-09-1966

    Application Number : 43319

    Regulatory Info : Cancelled

    Registration Country : Spain

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    Laboratorios Llorens Sa

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    Regulatory Info : Cancelled

    Registration Country : Spain

    Oxybuprocaine

    Brand Name : Prescaina Llorens Eye Drops

    Dosage Form : Eye Drop

    Dosage Strength :

    Packaging :

    Approval Date : 01-09-1966

    Application Number : 43318

    Regulatory Info : Cancelled

    Registration Country : Spain

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