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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.

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    IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.

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    medac CDMO: Tailored CDMO services for injectables in syringes, cartridges & vials – aseptic, reliable, flexible and a solution ahead.

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    PEG 3350; ELECTROLYTES

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    01 2Strides Pharma Science

    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

    09 1Dynapharm

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

    11 2Extrovis AG

    12 1Hanlim Pharmaceuticals Inc

    13 1Hospira, Inc.

    14 3JAMP PHARMA

    15 2Johnson & Johnson

    16 2Juno Pharmaceuticals Pty Ltd

    17 1MANTRA PHARMA INC

    18 1MEDEXUS PHARMACEUTICALS INC.

    19 1Medisca

    20 1Norgine

    21 8Norvium

    22 6Novel Laboratories, Inc.

    23 3Pendopharm

    24 4Perrigo Company plc

    25 1Pharmascience Inc.

    26 1SOLIS PHARMS

    27 2Salix Pharmaceuticals

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    29 1Taro Pharmaceutical Industries

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    01

    Strides Pharma Science

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    CPhI WW Frankfurt
    Booth # 9.1F6 & 9.1G41
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    Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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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

    Regulatory Info : RX

    Registration Country : USA

    Strides Pharma Science

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    02

    TAPI Technology & API Services

    Israel
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    CPhI WW Frankfurt
    Booth #6.1A32
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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

    Registration Country : USA

    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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    03

    Strides Pharma Science

    India
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    CPhI WW Frankfurt
    Booth # 9.1F6 & 9.1G41
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    Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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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

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    04

    BRAINTREE LABS

    U.S.A
    PREP
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    BRAINTREE LABS

    U.S.A
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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
    PREP
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    PREP
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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

    U.S.A
    PREP
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    PREP
    Not Confirmed
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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

    U.S.A
    PREP
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    PREP
    Not Confirmed
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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

    U.S.A
    PREP
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    PREP
    Not Confirmed
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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

    U.S.A
    PREP
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    PREP
    Not Confirmed
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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**

    Packaging :

    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
    PREP
    Not Confirmed
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    E-Z-EM Canada Inc, dba Therapex

    Canada
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    PREP
    Not Confirmed
    • fda
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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
    PREP
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    PREP
    Not Confirmed
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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
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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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    13

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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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    14

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
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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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    15

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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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    16

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
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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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    17

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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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    18

    Norvium

    U.S.A
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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
    PREP
    Not Confirmed
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    Norvium

    U.S.A
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    PREP
    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 : 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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    Salix Pharmaceuticals

    U.S.A
    PREP
    Not Confirmed
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    Salix Pharmaceuticals

    U.S.A
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    PREP
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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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