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    02 1TAPI Technology & API Services

    03 1ANGITA PHARMA INC.

    04 1Aralez Pharmaceuticals

    05 1Aurobindo Pharma Limited

    06 7BRAINTREE LABS

    07 1Bayer AG

    08 1CellChem Pharmaceuticals

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    10 1E-Z-EM Canada Inc, dba Therapex

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    Strides Pharma Science

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    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

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    TAPI Technology & API Services

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    Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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    Regulatory Info : DISCN

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

    Brand Name : GLYCOPREP

    Dosage Form : FOR SUSPENSION;ORAL

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

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    Approval Date : 1988-12-23

    Application Number : 72319

    Regulatory Info : DISCN

    Registration Country : USA

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    Strides Pharma Science

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    CPhI WW Frankfurt
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    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

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    Registration Country : USA

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    04

    BRAINTREE LABS

    U.S.A
    APGA Annual Conference
    Not Confirmed
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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

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    Approval Date : 1984-07-13

    Application Number : 19011

    Regulatory Info : RX

    Registration Country : USA

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    BRAINTREE LABS

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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

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    Approval Date : 1992-06-02

    Application Number : 19011

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    Registration Country : USA

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    06

    BRAINTREE LABS

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    BRAINTREE LABS

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    APGA Annual Conference
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    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

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    Approval Date : 1991-04-22

    Application Number : 19797

    Regulatory Info : RX

    Registration Country : USA

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    BRAINTREE LABS

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    BRAINTREE LABS

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    APGA Annual Conference
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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

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    Approval Date : 1994-11-18

    Application Number : 19797

    Regulatory Info : RX

    Registration Country : USA

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    08

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

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    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

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    Approval Date :

    Application Number : 21551

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    Registration Country : USA

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    09

    BRAINTREE LABS

    U.S.A
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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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    Not Confirmed
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    E-Z-EM Canada Inc, dba Therapex

    Canada
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    APGA Annual Conference
    Not Confirmed
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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
    APGA Annual Conference
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    APGA Annual Conference
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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

    Norvium

    U.S.A
    APGA Annual Conference
    Not Confirmed
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    Norvium

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    APGA Annual Conference
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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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    Norvium

    U.S.A
    APGA Annual Conference
    Not Confirmed
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    Norvium

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    APGA Annual Conference
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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

    U.S.A
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    Norvium

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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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    Norvium

    U.S.A
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    Not Confirmed
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    Norvium

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    APGA Annual Conference
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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

    U.S.A
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    Norvium

    U.S.A
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    APGA Annual Conference
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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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    Norvium

    U.S.A
    APGA Annual Conference
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    Norvium

    U.S.A
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    APGA Annual Conference
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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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    Norvium

    U.S.A
    APGA Annual Conference
    Not Confirmed
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    Norvium

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    APGA Annual Conference
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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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    19

    Norvium

    U.S.A
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    Not Confirmed
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    Norvium

    U.S.A
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    APGA Annual Conference
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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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    20

    Salix Pharmaceuticals

    U.S.A
    APGA Annual Conference
    Not Confirmed
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    Salix Pharmaceuticals

    U.S.A
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    APGA Annual Conference
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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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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