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    Sodium Benzoate

    ACTIVE PHARMA INGREDIENTS

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    01 1Ailex Pharma

    02 1B. Braun Medical

    03 1Bausch & Lomb Incorporated

    04 1Estilad

    05 2Maia Pharmaceuticals

    06 1Myungmoon Pharm. Co., LTD.

    07 2Navinta

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    01

    Ailex Pharma

    India
    Pharmtech & Ingredients
    Not Confirmed
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    Ailex Pharma

    India
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)

    Packaging :

    Approval Date : 2016-02-24

    Application Number : 207096

    Regulatory Info : RX

    Registration Country : USA

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    02

    B. Braun Medical

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    B. Braun Medical

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : UCEPHAN

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 100MG/ML;100MG/ML

    Packaging :

    Approval Date : 1987-12-23

    Application Number : 19530

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Bausch & Lomb Incorporated

    Canada
    Pharmtech & Ingredients
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    Bausch & Lomb Incorporated

    Canada
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    Regulatory Info : DISCN

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : AMMONUL

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)

    Packaging :

    Approval Date : 2005-02-17

    Application Number : 20645

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Estilad

    Canada
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    Estilad

    Canada
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    Regulatory Info :

    Registration Country : Canada

    Sodium DNA; Sodium Hyaluronate; Sodium Chloride; GLYCERIN; GLUCONOLACTONE; Sodium Benzoate; Calcium Gluconate

    Brand Name :

    Dosage Form : Solution

    Dosage Strength :

    Packaging :

    Approval Date :

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    Regulatory Info :

    Registration Country : Canada

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    05

    Maia Pharmaceuticals

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Maia Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)

    Packaging :

    Approval Date : 2017-05-08

    Application Number : 208521

    Regulatory Info : RX

    Registration Country : USA

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    06

    Maia Pharmaceuticals

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Maia Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (2GM/20ML;2GM/20ML)

    Packaging :

    Approval Date : 2021-06-10

    Application Number : 215025

    Regulatory Info : RX

    Registration Country : USA

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    07

    Myungmoon Pharm. Co., LTD.

    South Korea
    Pharmtech & Ingredients
    Not Confirmed
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    Myungmoon Pharm. Co., LTD.

    South Korea
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    Regulatory Info : Generic

    Registration Country : South Korea

    Caffeine; Sodium Benzoate

    Brand Name : Mezoca

    Dosage Form : INJECTION;

    Dosage Strength : 220MG/2ML;

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Korea

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    08

    Navinta

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Navinta

    U.S.A
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    Flag U.S.A
    Virtual Booth Virtual Booth
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    Regulatory Info : RX

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (5GM/50ML;5GM/50ML)

    Packaging :

    Approval Date : 2016-08-04

    Application Number : 205880

    Regulatory Info : RX

    Registration Country : USA

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    09

    Navinta

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Navinta

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

    Registration Country : USA

    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10%;10% (2GM/20ML; 2GM/20ML)

    Packaging :

    Approval Date : 2023-07-14

    Application Number : 217526

    Regulatory Info : RX

    Registration Country : USA

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