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    FAMAR CDMO- From early development to commercial manufacturing.

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    Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Together we can improve the quality of life

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    Sodium sulphate anhydrous

    ACTIVE PHARMA INGREDIENTS

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    01 2Aspen Pharmacare Holdings

    02 3Strides Pharma Science

    03 1TAPI Technology & API Services

    04 1ABC Farmaceutici SpA

    05 2Alfasigma

    06 1Alkem Laboratories

    07 1Annora Pharma

    08 1Aralez Pharmaceuticals

    09 4Azurity Pharma

    10 1BRAINTREE LABS

    11 1Bionpharma

    12 1Bohm Laboratories Sa

    13 2Cps Cito Pharma Services Gmbh

    14 1Dynapharm

    15 1E-Z-EM Canada Inc, dba Therapex

    16 1EJ Busuttil Ltd

    17 1Extrovis AG

    18 1GATOR PHARMS

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    20 1Hospira, Inc.

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    35 8Quagen Pharma

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    product-page Product Main Page

    01

    Aspen Pharmacare Holdings

    South Africa
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    IPPE
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : Originator

    Registration Country : South Africa

    Sodium sulphate anhydrous

    Brand Name : MOVIPREP

    Dosage Form : POW

    Dosage Strength : 7.5g

    Packaging : 1X1g

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

    Aspen API Comapny Banner

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    02

    Strides Pharma Science

    India
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    IPPE
    Not Confirmed
    • fda
    • EDQM
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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; 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

    Packaging :

    Approval Date : 2018-12-21

    Application Number : 204558

    Regulatory Info : RX

    Registration Country : USA

    Strides Pharma Science

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    03

    TAPI Technology & API Services

    Israel
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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

    Packaging :

    Approval Date : 1988-12-23

    Application Number : 72319

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Aspen Pharmacare Holdings

    South Africa
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    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Originator

    Registration Country : South Africa

    Sodium Sulphate Anhydrous

    Brand Name : Klean-prep

    Dosage Form : SAC

    Dosage Strength : 5.685g

    Packaging : 4X1g

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    05

    Strides Pharma Science

    India
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    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    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

    MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

    Brand Name : SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT

    Packaging :

    Approval Date : 2023-11-22

    Application Number : 215469

    Regulatory Info : RX

    Registration Country : USA

    Strides Pharma Science

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    06

    Strides Pharma Science

    India
    arrow
    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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    Regulatory Info :

    Registration Country : India

    Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

    Brand Name : Sodium Sulfate; Potassium Sulfate; Magnesium Sulfate

    Dosage Form : Oral Solution

    Dosage Strength : (17.5 g/3.13 g/1.6 g) per 6 ounces

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : India

    Strides Pharma Science

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    07

    Azurity Pharma

    U.S.A
    IPPE
    Not Confirmed
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    Azurity Pharma

    U.S.A
    arrow
    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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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    08

    Azurity Pharma

    U.S.A
    IPPE
    Not Confirmed
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    Azurity Pharma

    U.S.A
    arrow
    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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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    09

    Azurity Pharma

    U.S.A
    IPPE
    Not Confirmed
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    Azurity Pharma

    U.S.A
    arrow
    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE

    Brand Name : SUPREP BOWEL PREP KIT

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT

    Packaging :

    Approval Date : 2010-08-05

    Application Number : 22372

    Regulatory Info : RX

    Registration Country : USA

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    10

    E-Z-EM Canada Inc, dba Therapex

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

    Canada
    arrow
    IPPE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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
    IPPE
    Not Confirmed
    arrow

    Hospira, Inc.

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
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    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Quagen Pharma

    U.S.A
    IPPE
    Not Confirmed
    arrow

    Quagen Pharma

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

    Salix Pharmaceuticals

    U.S.A
    arrow
    IPPE
    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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