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    Approved Drug Products containing Eszopiclone listed in the FDA Orange Book. Original Data : FDA Website

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Ribobay has expertise in oligonucleotides from siRNA, Antisense Oligonucleotides, miRNAs, and aptamers & Oligonucleotides CXOs.

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    Eszopiclone

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    DR REDDYS

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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2014-04-15

    Application Number : 91024

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    DR REDDYS

    India
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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 2014-04-15

    Application Number : 91024

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    DR REDDYS

    India
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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

    Approval Date : 2014-04-15

    Application Number : 91024

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    ORBION PHARMS

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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2014-06-10

    Application Number : 91113

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    SUN PHARM

    India
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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2013-04-03

    Application Number : 91103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    SUN PHARM

    India
    AAPS 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 2013-04-03

    Application Number : 91103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    SUN PHARM

    India
    AAPS 2024
    Not Confirmed
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    SUN PHARM

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    Not Confirmed
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    RLD : No

    TE Code : AB

    ESZOPICLONE

    Brand Name : ESZOPICLONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

    Approval Date : 2013-04-03

    Application Number : 91103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    WAYLIS THERAP

    U.S.A
    AAPS 2024
    Not Confirmed
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    WAYLIS THERAP

    U.S.A
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    AAPS 2024
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    RLD : Yes

    TE Code : AB

    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2004-12-15

    Application Number : 21476

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    09

    WAYLIS THERAP

    U.S.A
    AAPS 2024
    Not Confirmed
    arrow

    WAYLIS THERAP

    U.S.A
    arrow
    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 2004-12-15

    Application Number : 21476

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    blank

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    10

    WAYLIS THERAP

    U.S.A
    AAPS 2024
    Not Confirmed
    arrow

    WAYLIS THERAP

    U.S.A
    arrow
    AAPS 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code : AB

    ESZOPICLONE

    Brand Name : LUNESTA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 3MG

    Approval Date : 2004-12-15

    Application Number : 21476

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF