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    Neostigmine Methyl Sulfate

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    Dr. Reddy's Laboratories

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    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2018-07-10

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    Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

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    Dosage Strength : 3MG/3ML (1MG/ML)

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    Approval Date : 2022-07-06

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    American Regent

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    Brand Name : NEOSTIGMINE METHYLSULFATE

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    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2018-05-04

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    American Regent

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    Amneal Pharmaceuticals

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    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2018-06-15

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    Amphastar Pharmaceuticals

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    Approval Date : 2017-09-25

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    Amphastar Pharmaceuticals

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    Brand Name : NEOSTIGMINE METHYLSULFATE

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    Approval Date : 2017-09-25

    Application Number : 209933

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    Avet Pharmaceuticals

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    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2022-11-25

    Application Number : 208230

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    Registration Country : USA

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    10

    Avet Pharmaceuticals

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    Approval Date : 2022-11-25

    Application Number : 208230

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    Registration Country : USA

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    11

    Exela Pharma Sciences, LLC.

    U.S.A
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    Brand Name : BLOXIVERZ

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    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2013-05-31

    Application Number : 204078

    Regulatory Info : RX

    Registration Country : USA

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    12

    Exela Pharma Sciences, LLC.

    U.S.A
    AACR Annual meeting
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    Exela Pharma Sciences, LLC.

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    Brand Name : BLOXIVERZ

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    Dosage Strength : 10MG/10ML (1MG/ML)

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    Approval Date : 2013-05-31

    Application Number : 204078

    Regulatory Info : RX

    Registration Country : USA

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    13

    Exela Pharma Sciences, LLC.

    U.S.A
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    Brand Name : BLOXIVERZ

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/5ML (1MG/ML)

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    Approval Date : 2023-10-27

    Application Number : 204078

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    14

    Fresenius Kabi USA

    U.S.A
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    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2015-01-08

    Application Number : 203629

    Regulatory Info : RX

    Registration Country : USA

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    Fresenius Kabi USA

    U.S.A
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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10MG/10ML (1MG/ML)

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    Approval Date : 2015-01-08

    Application Number : 203629

    Regulatory Info : RX

    Registration Country : USA

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    16

    Fresenius Kabi USA

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 3MG/3ML (1MG/ML)

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    Approval Date : 2018-09-18

    Application Number : 203629

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    17

    Hikma Pharmaceuticals

    United Kingdom
    AACR Annual meeting
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    Hikma Pharmaceuticals

    United Kingdom
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    AACR Annual meeting
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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2015-12-28

    Application Number : 207042

    Regulatory Info : RX

    Registration Country : USA

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    18

    Hikma Pharmaceuticals

    United Kingdom
    AACR Annual meeting
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    Hikma Pharmaceuticals

    United Kingdom
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    AACR Annual meeting
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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10MG/10ML (1MG/ML)

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    Approval Date : 2015-12-28

    Application Number : 207042

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    Registration Country : USA

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    19

    ENDO OPERATIONS

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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 5MG/10ML (0.5MG/ML)

    Packaging :

    Approval Date : 2017-04-26

    Application Number : 208405

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    Registration Country : USA

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    20

    ENDO OPERATIONS

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    AACR Annual meeting
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    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 10MG/10ML (1MG/ML)

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    Approval Date : 2017-04-26

    Application Number : 208405

    Regulatory Info : RX

    Registration Country : USA

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