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

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    Aurigene is a global leader in accelerating drug innovation through discovery, development & manufacturing.

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    Midas Pharma provides expertise in developing and supplying APIs, finished products, and intermediates.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

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    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1American Regent

    02 1Aurobindo Pharma Limited

    03 1Beloteca

    04 1Covidien, Ltd

    05 1Fresenius Kabi USA

    06 1Indoco Remedies Limited

    07 1MSN Laboratories

    08 1Meitheal Pharmaceuticals

    09 1Somerset Pharmaceuticals Inc

    10 1Viatris

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    American Regent

    U.S.A
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    American Regent

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    Regulatory Info : RX

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    ISOSULFAN BLUE

    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2023-05-17

    Application Number : 210294

    Regulatory Info : RX

    Registration Country : USA

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    Aurobindo Pharma Limited

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    Aurobindo Pharma Limited

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    Regulatory Info : DISCN

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    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2016-02-02

    Application Number : 206831

    Regulatory Info : DISCN

    Registration Country : USA

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    Beloteca

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    Beloteca

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    Regulatory Info : DISCN

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    ISOSULFAN BLUE

    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2019-01-16

    Application Number : 210714

    Regulatory Info : DISCN

    Registration Country : USA

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    Covidien, Ltd

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    Regulatory Info : DISCN

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    Brand Name : LYMPHAZURIN

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 18310

    Regulatory Info : DISCN

    Registration Country : USA

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    Fresenius Kabi USA

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    Regulatory Info : DISCN

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    ISOSULFAN BLUE

    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2022-09-08

    Application Number : 211869

    Regulatory Info : DISCN

    Registration Country : USA

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    Indoco Remedies Limited

    India
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    Regulatory Info : Generic

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    Dosage Form : Injection

    Dosage Strength : 0.01%

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    Regulatory Info : Generic

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    Meitheal Pharmaceuticals

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    Meitheal Pharmaceuticals

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    Regulatory Info : RX

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    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2021-11-03

    Application Number : 213130

    Regulatory Info : RX

    Registration Country : USA

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    MSN Laboratories

    India
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    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2022-09-16

    Application Number : 216090

    Regulatory Info : RX

    Registration Country : USA

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    Somerset Pharmaceuticals Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    ISOSULFAN BLUE

    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

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    Approval Date : 2019-07-12

    Application Number : 210558

    Regulatory Info : DISCN

    Registration Country : USA

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    Viatris

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    Regulatory Info : RX

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    ISOSULFAN BLUE

    Brand Name : ISOSULFAN BLUE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 50MG/5ML (10MG/ML)

    Packaging :

    Approval Date : 2010-07-20

    Application Number : 90874

    Regulatory Info : RX

    Registration Country : USA

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