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    01

    Xellia Pharmaceuticals ApS

    Denmark
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    Regulatory Info : RX

    Registration Country : USA

    POLYMYXIN B SULFATE

    Brand Name : POLYMYXIN B SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500,000 UNITS BASE/VIAL

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    Approval Date : 2014-01-15

    Application Number : 202766

    Regulatory Info : RX

    Registration Country : USA

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    02

    Sanofi

    France
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    Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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    Regulatory Info : Allowed

    Registration Country : Switzerland

    Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Diphtheria Toxoid; Tetanus Toxoid; Bordetella Pertussis Antigen; Inactivated Poliovirus Types 1, 2, 3; Polymyxin B; Haemophilus Influenzae Type B Polysaccharide Conjugated With Tetanus Toxoid; Pertussis Fimbriae

    Brand Name : Adacel-Polio

    Dosage Form : Suspension For Injection

    Dosage Strength :

    Packaging :

    Approval Date : 26/08/2022

    Application Number : 68110

    Regulatory Info : Allowed

    Registration Country : Switzerland

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    03

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE

    Brand Name : POLY-PRED

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.35% BASE;10,000 UNITS/ML;0.5%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50081

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Xellia Pharmaceuticals ApS

    Denmark
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    Regulatory Info : Generic

    Registration Country : Denmark

    Polymyxin B

    Brand Name :

    Dosage Form : Lyophilized Injection

    Dosage Strength : 500000Unit/Vial

    Packaging : 10 vials/pack, 25 vials/pack

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : Denmark

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    05

    Allergan Aesthetics

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    Brand Name : POLYTRIM

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : 10,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1988-10-20

    Application Number : 50567

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Alcon Inc

    U.S.A
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    Alcon Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : STATROL

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50344

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Alcon Inc

    U.S.A
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    Alcon Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : STATROL

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 3.5MG BASE/ML;16,250 UNITS/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50456

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    DELCOR ASSET

    U.S.A
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    DELCOR ASSET

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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : CORTISPORIN

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50416

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    DELCOR ASSET

    U.S.A
    RDD
    Not Confirmed
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    DELCOR ASSET

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : LUMI-SPORYN

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50417

    Regulatory Info : RX

    Registration Country : USA

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    10

    GSK

    United Kingdom
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    Not Confirmed
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN ZINC; POLYMYXIN B SULFATE

    Brand Name : POLYSPORIN

    Dosage Form : AEROSOL;TOPICAL

    Dosage Strength : 10,000 UNITS/GM;2,000,000 UNITS/GM

    Packaging :

    Approval Date : 1985-03-01

    Application Number : 50167

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    GSK

    United Kingdom
    RDD
    Not Confirmed
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : NEOSPORIN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : EQ 3.5MG BASE/GM;10,000 UNITS/GM

    Packaging :

    Approval Date : 1985-01-14

    Application Number : 50176

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Harrow

    U.S.A
    RDD
    Not Confirmed
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    Harrow

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : MAXITROL

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50023

    Regulatory Info : RX

    Registration Country : USA

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    13

    Pfizer Inc

    U.S.A
    RDD
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : CORTISPORIN

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-05-04

    Application Number : 50168

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : CORTISPORIN

    Dosage Form : SUSPENSION/DROPS;OPHTHALMIC

    Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50169

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Pfizer Inc

    U.S.A
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CHLORAMPHENICOL; HYDROCORTISONE ACETATE; POLYMYXIN B SULFATE

    Brand Name : OPHTHOCORT

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 10MG/GM;5MG/GM;10,000 UNITS/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50201

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Pfizer Inc

    U.S.A
    RDD
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CHLORAMPHENICOL; POLYMYXIN B SULFATE

    Brand Name : CHLOROMYXIN

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 1%;10,000 UNITS/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50203

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : CORTISPORIN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.5%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1985-08-09

    Application Number : 50218

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
    RDD
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : CORTISPORIN

    Dosage Form : SOLUTION/DROPS;OTIC

    Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50479

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sandoz B2B

    Switzerland
    RDD
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    Switzerland
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    Regulatory Info : RX

    Registration Country : USA

    DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE

    Brand Name : MAXITROL

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : 0.1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50065

    Regulatory Info : RX

    Registration Country : USA

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    20

    COMBE

    Country
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    COMBE

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    Regulatory Info : DISCN

    Registration Country : USA

    BACITRACIN; POLYMYXIN B SULFATE

    Brand Name : LANABIOTIC

    Dosage Form : DISC;TOPICAL

    Dosage Strength : 500 UNITS/GM;5,000 UNITS/GM

    Packaging :

    Approval Date : 1986-09-22

    Application Number : 50598

    Regulatory Info : DISCN

    Registration Country : USA

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