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    Magnesium sulfate in dextrose 5% in plastic container

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    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

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    Strides Pharma Science

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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

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    Strides Pharma Science

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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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    Azurity Pharma

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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

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    Baxter Healthcare Corporation

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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

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    Baxter Healthcare Corporation

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    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

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    Fresenius Kabi USA

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    MAGNESIUM SULFATE

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    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

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

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    Approval Date : 1986-09-08

    Application Number : 19316

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    Fresenius Kabi USA

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

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

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    Approval Date : 1986-09-08

    Application Number : 19316

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    Fresenius Kabi USA

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

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

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    Approval Date : 2016-01-29

    Application Number : 19316

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    Fresenius Kabi USA

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

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

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    Approval Date : 2016-01-29

    Application Number : 19316

    Regulatory Info : RX

    Registration Country : USA

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    Fresenius Kabi USA

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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 (1440ML)

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    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hospira, Inc.

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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/100ML (40MG/ML)

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    Approval Date : 1994-06-24

    Application Number : 20309

    Regulatory Info : RX

    Registration Country : USA

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    Hospira, Inc.

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

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

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    Approval Date : 1994-06-24

    Application Number : 20309

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    Registration Country : USA

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    Hospira, Inc.

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

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

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    Approval Date : 2007-01-26

    Application Number : 20309

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    Registration Country : USA

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    Hospira, Inc.

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

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

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    Approval Date : 1995-01-18

    Application Number : 20309

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    Hospira, Inc.

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

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

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    Approval Date : 1995-01-18

    Application Number : 20309

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    Hospira, Inc.

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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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    Hospira, Inc.

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    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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    Hospira, Inc.

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    MAGNESIUM SULFATE

    Brand Name : MAGNESIUM SULFATE

    Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS

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

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    Approval Date : 2000-04-25

    Application Number : 75151

    Regulatory Info : RX

    Registration Country : USA

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    Lukare medical

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    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.