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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Osmotica Pharmaceuticals

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    01 2DESVENLAFAXINE

    02 1DONEPEZIL HYDROCHLORIDE

    03 4HYDROMORPHONE HYDROCHLORIDE

    04 12METHYLPHENIDATE HYDROCHLORIDE

    05 3NIFEDIPINE

    06 1OMEGA-3-ACID ETHYL ESTERS TYPE A

    07 3OXYBUTYNIN CHLORIDE

    08 4VENLAFAXINE HYDROCHLORIDE

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    01

    Brand Name : KHEDEZLA

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : KHEDEZLA

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    DESVENLAFAXINE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : KHEDEZLA

    Dosage Strength : 50MG

    Approval Date : 2013-07-10

    Application Number : 204683

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : KHEDEZLA

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : KHEDEZLA

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code :

    DESVENLAFAXINE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : KHEDEZLA

    Dosage Strength : 100MG

    Approval Date : 2013-07-10

    Application Number : 204683

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : DONEPEZIL HYDROCHLOR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : DONEPEZIL HYDROCHLOR...

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    RLD : No

    TE Code :

    DONEPEZIL HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : DONEPEZIL HYDROCHLORIDE

    Dosage Strength : 23MG

    Approval Date : 2016-01-26

    Application Number : 203114

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
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    Brand Name : HYDROMORPHONE HYDROC...

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    RLD : No

    TE Code : AB

    HYDROMORPHONE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : HYDROMORPHONE HYDROCHLOR...

    Dosage Strength : 8MG

    Approval Date : 2016-07-07

    Application Number : 205629

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : HYDROMORPHONE HYDROC...

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    Fi Europe 2024
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    • fda
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    RLD : No

    TE Code : AB

    HYDROMORPHONE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : HYDROMORPHONE HYDROCHLOR...

    Dosage Strength : 12MG

    Approval Date : 2016-07-07

    Application Number : 205629

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    HYDROMORPHONE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : HYDROMORPHONE HYDROCHLOR...

    Dosage Strength : 16MG

    Approval Date : 2016-07-07

    Application Number : 205629

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : HYDROMORPHONE HYDROC...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    HYDROMORPHONE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : HYDROMORPHONE HYDROCHLOR...

    Dosage Strength : 32MG

    Approval Date : 2016-07-07

    Application Number : 205629

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    blank

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    08

    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
    arrow

    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AB

    METHYLPHENIDATE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : METHYLPHENIDATE HYDROCHL...

    Dosage Strength : 18MG

    Approval Date : 2017-07-28

    Application Number : 205327

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    • fda
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    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 : No

    TE Code : AB

    METHYLPHENIDATE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : METHYLPHENIDATE HYDROCHL...

    Dosage Strength : 27MG

    Approval Date : 2017-07-28

    Application Number : 205327

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Brand Name : METHYLPHENIDATE HYDR...

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    • 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 : No

    TE Code : AB

    METHYLPHENIDATE HYDROCHLORIDE

    Osmotica Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : METHYLPHENIDATE HYDROCHL...

    Dosage Strength : 36MG

    Approval Date : 2017-07-28

    Application Number : 205327

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    blank

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