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

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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Evonik Health Care is the innovation hub for leading life science companies

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    01 1Ethypharm

    02 2Strides Pharma Science

    03 1Adcock Ingram

    04 1Alkem Laboratories

    05 1Amanta Healthcare

    06 1Amgros I/S

    07 2Amneal Pharmaceuticals

    08 1Annora Pharma

    09 4Aspiro Pharma

    10 2Azurity Pharma

    11 4B. Braun Medical

    12 1B. Braun Melsungen AG

    13 1BRAINTREE LABS

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    15 12Baxter Healthcare Corporation

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    17 4Central Procurement & Supplies Unit

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    19 1DOMINION VETERINARY LABORATORIES LTD.

    20 2Demo S.A.

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    22 1Exela Pharma Sciences, LLC.

    23 8Fresenius Kabi AB Brunna

    24 4Fresenius Kabi Austria

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    26 5Fresenius SE & Co. KGaA

    27 1GATOR PHARMS

    28 2GLAND PHARMA LIMITED

    29 2Genchain Biotech

    30 6HQ SPCLT PHARMA

    31 9Hospira, Inc.

    32 1KIVIPharm

    33 1LABORATOIRES STEROP NV

    34 3Laboratorios ERN

    35 1Louis Widmer

    36 1Lukare medical

    37 3MONICO SpA

    38 1Mayoly Spindler

    39 1Medius Ag

    40 3Milla Pharmaceuticals

    41 2Montage Laboratories

    42 1Novel Laboratories, Inc.

    43 1PAC3 Limited

    44 1PAI HOLDINGS

    45 1PHARMOBEDIENT

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    01

    Ethypharm

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    Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

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    Magnesium Sulfate

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    Dosage Form : Ampoule

    Dosage Strength : 150MG/1ML

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    Registration Country : France

    Ethypharm

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    02

    Strides Pharma Science

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

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    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

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    Approval Date : 2023-11-22

    Application Number : 215469

    Regulatory Info : RX

    Registration Country : USA

    Strides Pharma Science

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    03

    Strides Pharma Science

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

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    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

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    Registration Country : India

    Strides Pharma Science

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    04

    Azurity Pharma

    U.S.A
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    Azurity Pharma

    U.S.A
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    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

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    Approval Date : 2010-08-05

    Application Number : 22372

    Regulatory Info : RX

    Registration Country : USA

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    05

    Baxter Healthcare Corporation

    U.S.A
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    Baxter Healthcare Corporation

    U.S.A
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    MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

    Brand Name : TIS-U-SOL IN PLASTIC CONTAINER

    Dosage Form : SOLUTION;IRRIGATION

    Dosage Strength : 20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

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    Approval Date : 1982-01-01

    Application Number : 18336

    Regulatory Info : RX

    Registration Country : USA

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    06

    Baxter Healthcare Corporation

    U.S.A
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    Baxter Healthcare Corporation

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM PHOSPHATE

    Brand Name : TIS-U-SOL

    Dosage Form : SOLUTION;IRRIGATION

    Dosage Strength : 20MG/100ML;40MG/100ML;6.25MG/100ML;800MG/100ML;8.75MG/100ML

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    Approval Date : 1982-02-19

    Application Number : 18508

    Regulatory Info : RX

    Registration Country : USA

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    07

    Fresenius Kabi USA

    U.S.A
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    Fresenius Kabi USA

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : 5GM/10ML (500MG/ML)

    Packaging :

    Approval Date : 1986-09-08

    Application Number : 19316

    Regulatory Info : RX

    Registration Country : USA

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    08

    Fresenius Kabi USA

    U.S.A
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : 1GM/2ML (500MG/ML)

    Packaging :

    Approval Date : 1986-09-08

    Application Number : 19316

    Regulatory Info : RX

    Registration Country : USA

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    09

    Fresenius Kabi USA

    U.S.A
    ASPEN
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : 10GM/20ML (500MG/ML)

    Packaging :

    Approval Date : 2016-01-29

    Application Number : 19316

    Regulatory Info : RX

    Registration Country : USA

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    10

    Fresenius Kabi USA

    U.S.A
    ASPEN
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASPEN
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : 25GM/50ML (500MG/ML)

    Packaging :

    Approval Date : 2016-01-29

    Application Number : 19316

    Regulatory Info : RX

    Registration Country : USA

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    11

    Fresenius Kabi USA

    U.S.A
    ASPEN
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASPEN
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    AMINO ACIDS; CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM GLYCEROPHOSPHATE; SOYBEAN OIL

    Brand Name : PERIKABIVEN IN PLASTIC CONTAINER

    Dosage Form : EMULSION;INTRAVENOUS

    Dosage Strength : 2.4%;20MG/100ML;6.8GM/100ML;68MG/100ML;124MG/100ML;170MG/100ML;105MG/100ML;3.5GM/100ML (1440ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    ASPEN
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASPEN
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4GM/100ML (40MG/ML)

    Packaging :

    Approval Date : 1994-06-24

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    ASPEN
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Regulatory Info : RX

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4GM/50ML (80MG/ML)

    Packaging :

    Approval Date : 1994-06-24

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    14

    Hospira, Inc.

    U.S.A
    ASPEN
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2GM/50ML (40MG/ML)

    Packaging :

    Approval Date : 2007-01-26

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
    ASPEN
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    Hospira, Inc.

    U.S.A
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    ASPEN
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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20GM/500ML (40MG/ML)

    Packaging :

    Approval Date : 1995-01-18

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    ASPEN
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASPEN
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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40GM/1000ML (40MG/ML)

    Packaging :

    Approval Date : 1995-01-18

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    17

    Hospira, Inc.

    U.S.A
    ASPEN
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASPEN
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    Regulatory Info : RX

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1GM/100ML

    Packaging :

    Approval Date : 1995-07-11

    Application Number : 20488

    Regulatory Info : RX

    Registration Country : USA

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    18

    Hospira, Inc.

    U.S.A
    ASPEN
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    Hospira, Inc.

    U.S.A
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    ASPEN
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2GM/100ML

    Packaging :

    Approval Date : 1995-07-11

    Application Number : 20488

    Regulatory Info : RX

    Registration Country : USA

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    19

    Hospira, Inc.

    U.S.A
    ASPEN
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    Hospira, Inc.

    U.S.A
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    ASPEN
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    Regulatory Info : RX

    Registration Country : USA

    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

    Dosage Strength : 5GM/10ML (500MG/ML)

    Packaging :

    Approval Date : 2000-04-25

    Application Number : 75151

    Regulatory Info : RX

    Registration Country : USA

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    Lukare medical

    U.S.A
    ASPEN
    Not Confirmed
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    Lukare medical

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM SULFATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE

    Brand Name : ELLIOTTS B SOLUTION

    Dosage Form : INJECTABLE;INTRATHECAL

    Dosage Strength : 0.2MG/ML;0.8MG/ML;0.3MG/ML;0.3MG/ML;1.9MG/ML;7.3MG/ML;0.2MG/ML

    Packaging :

    Approval Date : 1996-09-27

    Application Number : 20577

    Regulatory Info : RX

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.