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    Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate

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    Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    Dr. Reddy's Laboratories

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    Approval Date : 2017-09-25

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    Amring Pharma

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    Dosage Form : SOLUTION;INTRAVENOUS

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

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    Approval Date : 2018-08-22

    Application Number : 210989

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    Amring Pharma

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    Approval Date : 2018-08-22

    Application Number : 210989

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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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    Avet Pharmaceuticals

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    Approval Date : 2022-11-25

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    Biological E

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

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    Approval Date : 2019-05-13

    Application Number : 212512

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    Biological E

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    Approval Date : 2019-05-13

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    Exela Pharma Sciences, LLC.

    U.S.A
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    Dosage Strength : 5MG/10ML (0.5MG/ML)

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    Approval Date : 2013-05-31

    Application Number : 204078

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    Exela Pharma Sciences, LLC.

    U.S.A
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    Exela Pharma Sciences, LLC.

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    Approval Date : 2013-05-31

    Application Number : 204078

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    Exela Pharma Sciences, LLC.

    U.S.A
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    Exela Pharma Sciences, LLC.

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    Brand Name : BLOXIVERZ

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    Approval Date : 2023-10-27

    Application Number : 204078

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    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

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    Fresenius Kabi USA

    U.S.A
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    Approval Date : 2015-01-08

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    Fresenius Kabi USA

    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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    Hikma Pharmaceuticals

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

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    Approval Date : 2015-12-28

    Application Number : 207042

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    Registration Country : USA

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    23

    Hikma Pharmaceuticals

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2015-12-28

    Application Number : 207042

    Regulatory Info : RX

    Registration Country : USA

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    Meitheal Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Meitheal Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2021-04-05

    Application Number : 212804

    Regulatory Info : RX

    Registration Country : USA

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    25

    Umedica Laboratories

    India
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Umedica Laboratories

    India
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : RX

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    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2022-11-03

    Application Number : 212627

    Regulatory Info : RX

    Registration Country : USA

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    26

    Umedica Laboratories

    India
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Umedica Laboratories

    India
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    Regulatory Info : RX

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    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2022-11-03

    Application Number : 212627

    Regulatory Info : RX

    Registration Country : USA

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    27

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    Regulatory Info : RX

    Registration Country : USA

    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2017-04-26

    Application Number : 208405

    Regulatory Info : RX

    Registration Country : USA

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    28

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    Regulatory Info : RX

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    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2017-04-26

    Application Number : 208405

    Regulatory Info : RX

    Registration Country : USA

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    29

    ADAPTIS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ADAPTIS

    Country
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    Regulatory Info : RX

    Registration Country : USA

    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2021-10-01

    Application Number : 210652

    Regulatory Info : RX

    Registration Country : USA

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    30

    ADAPTIS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ADAPTIS

    Country
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : RX

    Registration Country : USA

    NEOSTIGMINE METHYLSULFATE

    Brand Name : NEOSTIGMINE METHYLSULFATE

    Dosage Form : SOLUTION;INTRAVENOUS

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

    Packaging :

    Approval Date : 2021-10-01

    Application Number : 210652

    Regulatory Info : RX

    Registration Country : USA

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