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    Approved Drug Products containing Sodium Polystyrene Sulfonate listed in the FDA Orange Book. Original Data : FDA Website

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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    Sodium Polystyrene Sulfonate

    ACTIVE PHARMA INGREDIENTS

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    01 3ANI PHARMS

    02 1BELCHER

    03 1CHARTWELL RX

    04 1CITRUSPHRMA

    05 2CMP PHARMA INC

    06 1CONCORDIA

    07 1EPIC PHARMA LLC

    08 1HIKMA

    09 2KVK TECH

    10 1MORTON GROVE

    11 2NUVO PHARMS INC

    12 1PAI HOLDINGS PHARM

    13 1ROXANE

    14 1UPSHER SMITH LABS

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    01

    ANI PHARMS

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    RLD : No

    TE Code : AA

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : KIONEX

    Dosage Form : SUSPENSION;ORAL, RECTAL

    Dosage Strength : 15GM/60ML

    Approval Date : 2007-09-17

    Application Number : 40028

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    ANI PHARMS

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    RLD : No

    TE Code : AA

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : KIONEX

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 454GM/BOT

    Approval Date : 1998-02-06

    Application Number : 40029

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    CMP PHARMA INC

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    RLD : Yes

    TE Code : AA

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : SPS

    Dosage Form : SUSPENSION;ORAL, RECTAL

    Dosage Strength : 15GM/60ML

    Approval Date : 1982-12-08

    Application Number : 87859

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AA

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    CONCORDIA

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    RLD : Yes

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : KAYEXALATE

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 453.6GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 11287

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    KVK TECH

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    RLD : No

    TE Code : AA

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : KALEXATE

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 454GM/BOT

    Approval Date : 2009-03-30

    Application Number : 40905

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    KVK TECH

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    RLD : No

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : KALEXATE

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 15GM/BOT

    Approval Date : 2015-04-03

    Application Number : 40905

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    MORTON GROVE

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    RLD : No

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : SODIUM POLYSTYRENE SULFONATE

    Dosage Form : SUSPENSION;ORAL, RECTAL

    Dosage Strength : 15GM/60ML

    Approval Date : 1984-09-11

    Application Number : 88717

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    PAI HOLDINGS PHARM

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    RLD : Yes

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : SODIUM POLYSTYRENE SULFONATE

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 453.6GM/BOT

    Approval Date : 1984-09-11

    Application Number : 88786

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    ROXANE

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    RLD : No

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : SODIUM POLYSTYRENE SULFONATE

    Dosage Form : SUSPENSION;ORAL, RECTAL

    Dosage Strength : 15GM/60ML

    Approval Date : 1983-11-17

    Application Number : 88453

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    CITRUSPHRMA

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    RLD : No

    TE Code :

    SODIUM POLYSTYRENE SULFONATE

    Brand Name : SODIUM POLYSTYRENE SULFONATE

    Dosage Form : POWDER;ORAL, RECTAL

    Dosage Strength : 454GM/BOT

    Approval Date : 2008-12-03

    Application Number : 40909

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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