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    List of All Manufacturers & Suppliers of 1000, PEG Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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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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    1000, PEG

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1Taro Pharmaceutical Industries

    02 2Strides Pharma Science

    03 1ANGITA PHARMA INC.

    04 1Alcon Inc

    05 1Aralez Pharmaceuticals

    06 1Aurobindo Pharma Limited

    07 7BRAINTREE LABS

    08 1Bayer AG

    09 1CellChem Pharmaceuticals

    10 1Dynapharm

    11 1E-Z-EM Canada Inc, dba Therapex

    12 2Extrovis AG

    13 1Hanlim Pharmaceuticals Inc

    14 1Hospira, Inc.

    15 1JAMP PHARMA

    16 2Johnson & Johnson

    17 1Juno Pharmaceuticals Pty Ltd

    18 1MANTRA PHARMA INC

    19 1MEDEXUS PHARMACEUTICALS INC.

    20 1Medisca

    21 8NORVIUM BIOSCIENCE

    22 1Norgine

    23 1Nostrum Laboratories

    24 6Novel Laboratories, Inc.

    25 3PENDOPHARM DIVISION OF DE PHARMASCIENCE INC

    26 4Perrigo Company plc

    27 1Pharmascience Inc.

    28 2Salix Pharmaceuticals

    29 1Sandoz B2B

    30 1Teva API

    31 1Teva Pharmaceutical Industries

    32 2Vintage Pharmaceuticals-Charlotte

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    01

    Strides Pharma Science

    India
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    CPhI Worldwide, Milan
    Booth #5C33
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : POLYETHYLENE GLYCOL 3350 AND ELECTROLYTES

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

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    Approval Date : 2018-12-21

    Application Number : 204558

    Regulatory Info : RX

    Registration Country : USA

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    02

    Taro Pharmaceutical Industries

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    Brand Name : PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

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    Approval Date : 2024-06-28

    Application Number : 207498

    Regulatory Info : RX

    Registration Country : USA

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    03

    Strides Pharma Science

    India
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    CPhI Worldwide, Milan
    Booth #5C33
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : PEG-3350, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CHLORIDE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

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    Approval Date : 2015-04-13

    Application Number : 204559

    Regulatory Info : RX

    Registration Country : USA

    Strides Pharma Science

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    04

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GOLYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

    Packaging :

    Approval Date : 1984-07-13

    Application Number : 19011

    Regulatory Info : RX

    Registration Country : USA

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    05

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : GOLYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET

    Packaging :

    Approval Date : 1992-06-02

    Application Number : 19011

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    BRAINTREE LABS

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    BRAINTREE LABS

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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : NULYTELY

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

    Packaging :

    Approval Date : 1991-04-22

    Application Number : 19797

    Regulatory Info : RX

    Registration Country : USA

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    07

    BRAINTREE LABS

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    Regulatory Info : RX

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : NULYTELY-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT

    Packaging :

    Approval Date : 1994-11-18

    Application Number : 19797

    Regulatory Info : RX

    Registration Country : USA

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    08

    BRAINTREE LABS

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    BRAINTREE LABS

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    Regulatory Info :

    Registration Country : USA

    BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : HALFLYTELY

    Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM

    Packaging :

    Approval Date :

    Application Number : 21551

    Regulatory Info :

    Registration Country : USA

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    09

    BRAINTREE LABS

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    BRAINTREE LABS

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    Regulatory Info : DISCN

    Registration Country : USA

    BISACODYL; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE

    Brand Name : HALFLYTELY

    Dosage Form : FOR SOLUTION, TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 5MG,N/A;N/A,210GM;N/A,0.74GM;N/A,2.86GM;N/A,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-07-16

    Application Number : 21551

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    E-Z-EM Canada Inc, dba Therapex

    Canada
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    E-Z-EM Canada Inc, dba Therapex

    Canada
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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : E-Z-EM PREP LYTE

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT

    Packaging :

    Approval Date : 1988-11-21

    Application Number : 71278

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
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    Hospira, Inc.

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE

    Brand Name : OCL

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 6GM/100ML;75MG/100ML;168MG/100ML;146MG/100ML;1.29GM/100ML

    Packaging :

    Approval Date : 1986-04-30

    Application Number : 19284

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Salix Pharmaceuticals

    U.S.A
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    Salix Pharmaceuticals

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    Regulatory Info : RX

    Registration Country : USA

    ASCORBIC ACID; POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM ASCORBATE; SODIUM CHLORIDE; SODIUM SULFATE

    Brand Name : MOVIPREP

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 4.7GM;100GM;1.015GM;5.9GM;2.691GM;7.5GM

    Packaging :

    Approval Date : 2006-08-02

    Application Number : 21881

    Regulatory Info : RX

    Registration Country : USA

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    13

    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/PACKET;2.82GM/PACKET;6.36GM/PACKET;5.53GM/PACKET;21.5GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 120GM/PACKET;1.49GM/PACKET;3.36GM/PACKET;2.92GM/PACKET;11.36GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 360GM/PACKET;4.47GM/PACKET;10.08GM/PACKET;8.76GM/PACKET;34.08GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-10-26

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1987-06-12

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-14

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE-FLAVORED

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-14

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 227.1GM/BOT;2.82GM/BOT;6.36GM/BOT;5.53GM/BOT;21.5GM/BOT **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1989-01-31

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

    Registration Country : USA

    POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS

    Brand Name : COLYTE WITH FLAVOR PACKS

    Dosage Form : FOR SOLUTION;ORAL

    Dosage Strength : 240GM/BOT;2.98GM/BOT;6.72GM/BOT;5.84GM/BOT;22.72GM/BOT

    Packaging :

    Approval Date : 1998-10-08

    Application Number : 18983

    Regulatory Info : DISCN

    Registration Country : USA

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