Please Wait
Applying Filters...
menu
    • menu
    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

    Virtual Booth

    Contact Supplier

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

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

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

    Virtual Booth

    Contact Supplier

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

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    Menu

    Magnesium sulfate, unspecified

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

    PharmaCompass
    $ API Ref.Price (USD/KG) : 34Xls

    Filters

    clear-filterReset all filters
    Filters Filter
    Cross PopUp
    FILTER :

    filter clear-filterReset all filters

    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

    41 3Viatris

    42 1Zuma Pharma

    43 1Blank

    filter clear-filterReset all filters

    filter clear-filterReset all filters

    filter clear-filterReset all filters

    filter clear-filterReset all filters

    PharmaCompass
    ListList of Suppliers
    refreshReset Filter
    refresh Reset Filter
    Price Info Price Info
    product-page Product Main Page

    01

    Ethypharm

    France
    arrow
    CPhI WW Frankfurt
    Booth #5.0D100
    • fda
    • EDQM
    • WHO-GMP

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

    Contact Supplier Contact Supplier
    Flag France
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info :

    Registration Country : France

    Magnesium Sulfate

    Brand Name :

    Dosage Form : Ampoule

    Dosage Strength : 150MG/1ML

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : France

    Ethypharm

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    02

    Strides Pharma Science

    India
    arrow
    CPhI India 2024
    Attending
    • fda
    • EDQM
    • WHO-GMP

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

    Contact Supplier Contact Supplier
    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    03

    Taro Pharmaceutical Industries

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Contact Supplier Contact Supplier
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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 : 2024-03-19

    Application Number : 206431

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    04

    Baxter Healthcare Corporation

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Baxter Healthcare Corporation

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18336

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    05

    Baxter Healthcare Corporation

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Baxter Healthcare Corporation

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Packaging :

    Approval Date : 1982-02-19

    Application Number : 18508

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    06

    BRAINTREE LABS

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    BRAINTREE LABS

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    07

    BRAINTREE LABS

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    BRAINTREE LABS

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    Packaging :

    Approval Date : 2013-01-18

    Application Number : 203595

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    08

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    09

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    10

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    11

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    12

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    13

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    14

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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 (2400ML)

    Packaging :

    Approval Date : 2014-08-25

    Application Number : 200656

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    15

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    16

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    17

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    18

    Fresenius Kabi USA

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Fresenius Kabi USA

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    19

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    20

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    21

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    22

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    23

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    24

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    25

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    26

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    27

    Hospira, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Hospira, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    28

    Lukare medical

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Lukare medical

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    29

    Novel Laboratories, Inc.

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Novel Laboratories, Inc.

    U.S.A
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    30

    Perrigo Company plc

    Ireland
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Perrigo Company plc

    Ireland
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag Ireland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    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

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF