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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Acetyl Sulfisoxazole

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    REF. STANDARDS & IMPURITIES

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    01 1ALRA

    02 1Barr Laboratories

    03 1Eli Lilly

    04 3F. Hoffmann-La Roche

    05 1Ross Lab

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    01

    ALRA

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    ALRA

    United Kingdom
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    Antibody Engineering
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    Regulatory Info : DISCN

    Registration Country : USA

    ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL

    Brand Name : ERYZOLE

    Dosage Form : GRANULE;ORAL

    Dosage Strength : EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 62758

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Barr Laboratories

    U.S.A
    Antibody Engineering
    Not Confirmed
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    Barr Laboratories

    U.S.A
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    Antibody Engineering
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    Regulatory Info : DISCN

    Registration Country : USA

    ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL

    Brand Name : ERYTHROMYCIN ETHYLSUCCINATE AND SULFISOXAZOLE ACETYL

    Dosage Form : GRANULE;ORAL

    Dosage Strength : EQ 200MG BASE/5ML;EQ 600MG BASE/5ML

    Packaging :

    Approval Date : 1988-05-20

    Application Number : 62759

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Eli Lilly

    U.S.A
    Antibody Engineering
    Not Confirmed
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    Eli Lilly

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    ERYTHROMYCIN ESTOLATE; SULFISOXAZOLE ACETYL

    Brand Name : ILOSONE SULFA

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML;EQ 600MG BASE/5ML

    Packaging :

    Approval Date : 1989-09-29

    Application Number : 50599

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    F. Hoffmann-La Roche

    Switzerland
    Antibody Engineering
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFISOXAZOLE ACETYL

    Brand Name : GANTRISIN

    Dosage Form : SYRUP;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9182

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    F. Hoffmann-La Roche

    Switzerland
    Antibody Engineering
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    Antibody Engineering
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFISOXAZOLE ACETYL

    Brand Name : GANTRISIN PEDIATRIC

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9182

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    F. Hoffmann-La Roche

    Switzerland
    Antibody Engineering
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    Antibody Engineering
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    Regulatory Info : DISCN

    Registration Country : USA

    SULFISOXAZOLE ACETYL

    Brand Name : LIPO GANTRISIN

    Dosage Form : EMULSION;ORAL

    Dosage Strength : EQ 1GM BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9182

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Ross Lab

    U.S.A
    Antibody Engineering
    Not Confirmed
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    Ross Lab

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL

    Brand Name : PEDIAZOLE

    Dosage Form : GRANULE;ORAL

    Dosage Strength : EQ 200MG BASE/5ML;EQ 600MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50529

    Regulatory Info : DISCN

    Registration Country : USA

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