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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    Sodium Phenylacetate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    PATENTS & EXCLUSIVITIES

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    01 1Ailex Pharma

    02 1B. Braun Medical

    03 1Bausch & Lomb Incorporated

    04 2Maia Pharmaceuticals

    05 2Navinta

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    Ailex Pharma

    India
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    Ailex Pharma

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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)

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    Approval Date : 2016-02-24

    Application Number : 207096

    Regulatory Info : RX

    Registration Country : USA

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    B. Braun Medical

    U.S.A
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    B. Braun Medical

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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

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    Approval Date : 1987-12-23

    Application Number : 19530

    Regulatory Info : DISCN

    Registration Country : USA

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    Bausch & Lomb Incorporated

    Canada
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    Regulatory Info : DISCN

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    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : AMMONUL

    Dosage Form : SOLUTION;INTRAVENOUS

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

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    Approval Date : 2005-02-17

    Application Number : 20645

    Regulatory Info : DISCN

    Registration Country : USA

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    Maia Pharmaceuticals

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    Regulatory Info : RX

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    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

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    Approval Date : 2017-05-08

    Application Number : 208521

    Regulatory Info : RX

    Registration Country : USA

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    Maia Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

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    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

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    Approval Date : 2021-06-10

    Application Number : 215025

    Regulatory Info : RX

    Registration Country : USA

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    Navinta

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    Regulatory Info : RX

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    SODIUM BENZOATE; SODIUM PHENYLACETATE

    Brand Name : SODIUM PHENYLACETATE AND SODIUM BENZOATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

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    Approval Date : 2016-08-04

    Application Number : 205880

    Regulatory Info : RX

    Registration Country : USA

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    Navinta

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    Navinta

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    Regulatory Info : RX

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    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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