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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    xyz-pharma-m-2024-10-07

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Magnesium Sulfate

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    01 1Taro Pharmaceutical Industries

    02 1Ethypharm

    03 1Strides Pharma Science

    04 1Alkem Laboratories

    05 2Amneal Pharmaceuticals

    06 1Annora Pharma

    07 4B. Braun Medical

    08 1B. Braun Melsungen AG

    09 3BRAINTREE LABS

    10 1Bahrain Pharma

    11 8Baxter Healthcare Corporation

    12 1Bionpharma

    13 1Cooper Pharma Limited

    14 1DOMINION VETERINARY LABORATORIES LTD.

    15 2Demo S.A.

    16 1Eurofarma Laboratorios S.A

    17 1Exela Pharma Sciences, LLC.

    18 1Fresenius Kabi AB Brunna

    19 4Fresenius Kabi Austria

    20 17Fresenius Kabi USA

    21 5Fresenius SE & Co. KGaA

    22 1GATOR PHARMS

    23 2GLAND PHARMA LIMITED

    24 2Genchain Biotech

    25 2Grindeks AS

    26 6HQ SPCLT PHARMA

    27 9Hospira, Inc.

    28 1KIVIPharm

    29 1Lukare medical

    30 3MONICO SpA

    31 3Milla Pharmaceuticals

    32 1Novel Laboratories, Inc.

    33 1PAI HOLDINGS

    34 1Perrigo Company plc

    35 1Polifarma

    36 5SALF SpA

    37 1Sandoz B2B

    38 1United Biomed

    39 2Vefa Ilac

    40 1Verve Human Care Laboratories

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    01

    Ethypharm

    France
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    CPhI WW Frankfurt
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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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    Registration Country : France

    Magnesium Sulfate

    Brand Name :

    Dosage Form : Ampoule

    Dosage Strength : 150MG/1ML

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    Approval Date :

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    Registration Country : France

    Ethypharm

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    02

    Strides Pharma Science

    India
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    CPhI India 2024
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    Regulatory Info : RX

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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

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    03

    Taro Pharmaceutical Industries

    U.S.A
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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

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    Approval Date : 2024-03-19

    Application Number : 206431

    Regulatory Info : RX

    Registration Country : USA

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    04

    Baxter Healthcare Corporation

    U.S.A
    Pharmtech & Ingredients
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    Baxter Healthcare Corporation

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
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    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

    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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    05

    Baxter Healthcare Corporation

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
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    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

    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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    06

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

    U.S.A
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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

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    Approval Date : 2010-08-05

    Application Number : 22372

    Regulatory Info : RX

    Registration Country : USA

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    07

    BRAINTREE LABS

    U.S.A
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    BRAINTREE LABS

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

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

    Brand Name : SUCLEAR

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 1.6GM/BOT,3.13GM/BOT,17.5GM/BOT,N/A,N/A,N/A,N/A;N/A,N/A,N/A,210GM,0.74GM,2.86GM,5.6GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reason

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    Approval Date : 2013-01-18

    Application Number : 203595

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
    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 : 5GM/10ML (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
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
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    Regulatory Info : RX

    Registration Country : USA

    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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    10

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
    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 : 10GM/20ML (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
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
    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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    12

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
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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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    13

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    Pharmtech & Ingredients
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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 (1920ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    14

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

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    Regulatory Info : RX

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    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 (2400ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    15

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

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    Pharmtech & Ingredients
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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 : KABIVEN IN PLASTIC CONTAINER

    Dosage Form : EMULSION;INTRAVENOUS

    Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML ;147MG/100ML;3.9GM/100ML (1026ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    16

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

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    Pharmtech & Ingredients
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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 : KABIVEN IN PLASTIC CONTAINER

    Dosage Form : EMULSION;INTRAVENOUS

    Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (1540ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    17

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

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    Pharmtech & Ingredients
    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 : KABIVEN IN PLASTIC CONTAINER

    Dosage Form : EMULSION;INTRAVENOUS

    Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2053ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    18

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Fresenius Kabi USA

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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 : KABIVEN IN PLASTIC CONTAINER

    Dosage Form : EMULSION;INTRAVENOUS

    Dosage Strength : 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2566ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    19

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    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 : 4GM/100ML (40MG/ML)

    Packaging :

    Approval Date : 1994-06-24

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    20

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    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/50ML (80MG/ML)

    Packaging :

    Approval Date : 1994-06-24

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    21

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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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 : 2GM/50ML (40MG/ML)

    Packaging :

    Approval Date : 2007-01-26

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    22

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    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 : 20GM/500ML (40MG/ML)

    Packaging :

    Approval Date : 1995-01-18

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    23

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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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 : 40GM/1000ML (40MG/ML)

    Packaging :

    Approval Date : 1995-01-18

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    24

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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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 : 1GM/100ML

    Packaging :

    Approval Date : 1995-07-11

    Application Number : 20488

    Regulatory Info : RX

    Registration Country : USA

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    25

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Not Confirmed
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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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    26

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    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 : 5GM/10ML (500MG/ML)

    Packaging :

    Approval Date : 2000-04-25

    Application Number : 75151

    Regulatory Info : RX

    Registration Country : USA

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    27

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Hospira, Inc.

    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 : 2015-05-14

    Application Number : 202411

    Regulatory Info : RX

    Registration Country : USA

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    28

    Lukare medical

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Lukare medical

    U.S.A
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    Not Confirmed
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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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    29

    Novel Laboratories, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Novel Laboratories, Inc.

    U.S.A
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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 : 2017-02-23

    Application Number : 202511

    Regulatory Info : RX

    Registration Country : USA

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    30

    Perrigo Company plc

    Ireland
    Pharmtech & Ingredients
    Not Confirmed
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    Perrigo Company plc

    Ireland
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    Not Confirmed
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    Regulatory Info :

    Registration Country : USA

    MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE

    Brand Name : MAGNESIUM SULFATE ANHYDROUS; POTASSIUM SULFATE; SODIUM SULFATE

    Dosage Form : SOLUTION;ORAL

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

    Packaging :

    Approval Date :

    Application Number : 203102

    Regulatory Info :

    Registration Country : USA

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