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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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    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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    CAS-7681-82-5

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 3CARDINAL HEALTH 418

    02 2CURIUM

    03 3GE HEALTHCARE

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    01

    CARDINAL HEALTH 418

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    CARDINAL HEALTH 418

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    RLD : Yes

    TE Code : AA

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100uCi

    Approval Date : 1982-05-27

    Application Number : 18671

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AA

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    02

    CARDINAL HEALTH 418

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    CARDINAL HEALTH 418

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    RLD : Yes

    TE Code : AA

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200uCi

    Approval Date : 1982-05-27

    Application Number : 18671

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AA

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    03

    CARDINAL HEALTH 418

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    CARDINAL HEALTH 418

    U.S.A
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    Pharma, Lab & Chemical Expo
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    RLD : No

    TE Code :

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 400uCi

    Approval Date : 1982-05-27

    Application Number : 18671

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    GE HEALTHCARE

    United Kingdom
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    GE HEALTHCARE

    United Kingdom
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    RLD : No

    TE Code :

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100uCi

    Approval Date : 1982-01-01

    Application Number : 17630

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    05

    GE HEALTHCARE

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    GE HEALTHCARE

    United Kingdom
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    RLD : No

    TE Code :

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 2mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 17630

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    GE HEALTHCARE

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    GE HEALTHCARE

    United Kingdom
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    RLD : No

    TE Code :

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200uCi

    Approval Date : 1993-01-08

    Application Number : 17630

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    CURIUM

    Belgium
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    CURIUM

    Belgium
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    Not Confirmed
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    RLD : No

    TE Code : AA

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100uCi

    Approval Date : 1989-02-28

    Application Number : 71909

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    08

    CURIUM

    Belgium
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    CURIUM

    Belgium
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    RLD : No

    TE Code : AA

    SODIUM IODIDE I-123

    Brand Name : SODIUM IODIDE I 123

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200uCi

    Approval Date : 1989-02-28

    Application Number : 71910

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

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