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    Dr. Reddy's Laboratories

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    Hikma Pharmaceuticals

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    Hikma Pharmaceuticals

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    Lupin Ltd

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    Approval Date : 2011-09-13

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    Lupin Ltd

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    Lupin Ltd

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    OrBion Pharmaceuticals

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    OrBion Pharmaceuticals

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    Sun Pharmaceutical Industries Limit...

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    Sun Pharmaceutical Industries Limit...

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    Sun Pharmaceutical Industries Limit...

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    Teva Pharmaceutical Industries

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    Approval Date : 2011-05-23

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    Registration Country : USA

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    Viatris

    U.S.A
    BePharma
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    Viatris

    U.S.A
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    BePharma
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    • EDQM
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    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2013-03-26

    Application Number : 91151

    Regulatory Info : RX

    Registration Country : USA

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    27

    Viatris

    U.S.A
    BePharma
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    U.S.A
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    Regulatory Info : RX

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    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

    Packaging :

    Approval Date : 2013-03-26

    Application Number : 91151

    Regulatory Info : RX

    Registration Country : USA

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    28

    Waylis Therapeutics

    U.S.A
    BePharma
    Not Confirmed
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    Waylis Therapeutics

    U.S.A
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    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 2004-12-15

    Application Number : 21476

    Regulatory Info : RX

    Registration Country : USA

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    29

    Waylis Therapeutics

    U.S.A
    BePharma
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    Waylis Therapeutics

    U.S.A
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    Regulatory Info : RX

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    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2004-12-15

    Application Number : 21476

    Regulatory Info : RX

    Registration Country : USA

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    30

    Waylis Therapeutics

    U.S.A
    BePharma
    Not Confirmed
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    Waylis Therapeutics

    U.S.A
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    BePharma
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    Regulatory Info : RX

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    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

    Packaging :

    Approval Date : 2004-12-15

    Application Number : 21476

    Regulatory Info : RX

    Registration Country : USA

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