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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.

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    Inke S.A: APIs manufacturing plant.

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    Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Neomycin Sulfate

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    01 1AbbVie Inc

    02 1Allergan Aesthetics

    03 1Polfa Tarchomin

    04 1ALFA INTES (IND.TER.SPLENDORE)

    05 1ALTANA

    06 1AVIV PHARMA

    07 4Actavis Inc

    08 1Adastra Pharmaceuticals

    09 6Alcon Inc

    10 2Antibiotice

    11 1Associated Biotech

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    13 19Bausch & Lomb Incorporated

    14 2Bausch Health

    15 4Bayer AG

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    26 3Eli Lilly

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    29 2Flagship Biotech International Pvt. Ltd

    30 2Fougera Pharmaceuticals Inc.

    31 5GSK

    32 1Glenmark Pharmaceuticals

    33 1Hanlim Pharmaceuticals Inc

    34 1Harrow

    35 2Kolmar Korea Co., Ltd.

    36 1LABORATORIOS NORMON SA

    37 1Laboratorios ERN

    38 1Laboratorios Llorens Sa

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    53 3Padagis

    54 27Pfizer Inc

    55 1Pharmacorp (Pty) Ltd

    56 3Pharmaderm

    57 2Qilu Animal Health Products

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    59 1Reig Jofre

    60 1S.A. Alcon-Couvreur N.V.

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    62 6Sandoz B2B

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    01

    AbbVie Inc

    U.S.A
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    Regulatory Info : Originator

    Registration Country : South Africa

    Neomycin sulphate

    Brand Name : FML Neo Liquifilm Ophthalmic Suspension

    Dosage Form : OPD

    Dosage Strength : 5mg/ml

    Packaging : 5X1mg/ml

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    02

    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

    Abbvie CB

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    03

    Polfa Tarchomin

    Poland
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    Virtual BoothPolfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Regulatory Info : Dossier Available

    Registration Country : Poland

    Neomycin Sulfate

    Brand Name :

    Dosage Form : Suspension for Cutaneous Spray

    Dosage Strength : 11.72MG/GM

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Dossier Available

    Registration Country : Poland

    Polfa Tarchomin

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    04

    Alcon Inc

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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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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    05

    Bayer AG

    Germany
    Aus. Peptide Conference
    Not Confirmed
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    Bayer AG

    Germany
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    Aus. Peptide Conference
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1984-06-05

    Application Number : 50237

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bayer AG

    Germany
    Aus. Peptide Conference
    Not Confirmed
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    Bayer AG

    Germany
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    Aus. Peptide Conference
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.5%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1984-06-05

    Application Number : 50237

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Bayer AG

    Germany
    Aus. Peptide Conference
    Not Confirmed
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    Bayer AG

    Germany
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    Regulatory Info : DISCN

    Registration Country : USA

    ACETIC ACID, GLACIAL; HYDROCORTISONE; NEOMYCIN SULFATE

    Brand Name : NEO-CORT-DOME

    Dosage Form : SUSPENSION/DROPS;OTIC

    Dosage Strength : 2%;1%;EQ 0.35% BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50238

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Eli Lilly

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Eli Lilly

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    FLURANDRENOLIDE; NEOMYCIN SULFATE

    Brand Name : CORDRAN N

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50345

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Eli Lilly

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Eli Lilly

    U.S.A
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    Aus. Peptide Conference
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    Regulatory Info : DISCN

    Registration Country : USA

    FLURANDRENOLIDE; NEOMYCIN SULFATE

    Brand Name : CORDRAN N

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.05%;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50346

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    GSK

    United Kingdom
    Aus. Peptide Conference
    Not Confirmed
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    GSK

    United Kingdom
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    Aus. Peptide Conference
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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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    11

    Harrow

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Harrow

    U.S.A
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    Aus. Peptide Conference
    Not Confirmed
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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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    12

    Merck & Co

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Merck & Co

    U.S.A
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    Aus. Peptide Conference
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

    Brand Name : NEODECADRON

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50322

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Merck & Co

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

    Brand Name : NEODECADRON

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50324

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Merck & Co

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE; PREDNISOLONE SODIUM PHOSPHATE

    Brand Name : NEO-HYDELTRASOL

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 3.5MG BASE/GM;EQ 0.25% PHOSPHATE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50378

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Pfizer Inc

    U.S.A
    Aus. Peptide Conference
    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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    16

    Pfizer Inc

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Aus. Peptide Conference
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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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    17

    Pfizer Inc

    U.S.A
    Aus. Peptide Conference
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Aus. Peptide Conference
    Not Confirmed
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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
    Aus. Peptide Conference
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Aus. Peptide Conference
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    NEOMYCIN SULFATE

    Brand Name : MYCIFRADIN

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 87.5MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50285

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sandoz B2B

    Switzerland
    Aus. Peptide Conference
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    Aus. Peptide Conference
    Not Confirmed
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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

    PH HEALTH

    Country
    Aus. Peptide Conference
    Not Confirmed
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    PH HEALTH

    Country
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    Aus. Peptide Conference
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    COLISTIN SULFATE; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; THONZONIUM BROMIDE

    Brand Name : COLY-MYCIN S

    Dosage Form : SUSPENSION/DROPS;OTIC

    Dosage Strength : EQ 3MG BASE/ML;10MG/ML;EQ 3.3MG BASE/ML;0.5MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50356

    Regulatory Info : RX

    Registration Country : USA

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