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    List of All Manufacturers & Suppliers of AGN-PC-0JKHFR Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    AGN-PC-0JKHFR

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    PRICE INFORMATION

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

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    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

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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 1Lannett Company, Inc.

    30 1Lukare medical

    31 3MONICO SpA

    32 3Milla Pharmaceuticals

    33 1Novel Laboratories, Inc.

    34 1Perrigo Company plc

    35 1Polifarma

    36 5SALF SpA

    37 1Sandoz B2B

    38 2Vefa Ilac

    39 1Verve Human Care Laboratories

    40 3Viatris

    41 1Zuma Pharma

    42 1Blank

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    01

    Ethypharm

    France
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    CPhI Worldwide, Milan
    Booth #7G84
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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 : 0.5MG

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : France

    Ethypharm

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    02

    Strides Pharma Science

    India
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    CPhI Worldwide, Milan
    Booth #5C33
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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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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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    03

    Taro Pharmaceutical Industries

    U.S.A
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    ASC 2024
    Not Confirmed
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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 : 2024-03-19

    Application Number : 206431

    Regulatory Info : RX

    Registration Country : USA

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    04

    Baxter Healthcare Corporation

    U.S.A
    ASC 2024
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    ASC 2024
    Not Confirmed
    • fda
    • EDQM
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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

    Packaging :

    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
    ASC 2024
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
    arrow
    ASC 2024
    Not Confirmed
    • fda
    • EDQM
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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

    Packaging :

    Approval Date : 1982-02-19

    Application Number : 18508

    Regulatory Info : RX

    Registration Country : USA

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    06

    BRAINTREE LABS

    U.S.A
    ASC 2024
    Not Confirmed
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    BRAINTREE LABS

    U.S.A
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    ASC 2024
    Not Confirmed
    • fda
    • EDQM
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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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    07

    Fresenius Kabi USA

    U.S.A
    ASC 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASC 2024
    Not Confirmed
    • fda
    • EDQM
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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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    09

    Fresenius Kabi USA

    U.S.A
    ASC 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
    arrow
    ASC 2024
    Not Confirmed
    • fda
    • EDQM
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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
    ASC 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    ASC 2024
    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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    12

    Hospira, Inc.

    U.S.A
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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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    14

    Hospira, Inc.

    U.S.A
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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 : 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
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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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    19

    Hospira, Inc.

    U.S.A
    ASC 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASC 2024
    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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    20

    Lukare medical

    U.S.A
    ASC 2024
    Not Confirmed
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    Lukare medical

    U.S.A
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    ASC 2024
    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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