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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Dexmethylphenidate Hydrochloride

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    01 8Granules India Limited

    02 3ABHAI INC

    03 8Adare Pharma Solutions

    04 8Ajanta Pharma Limited

    05 3Alkem Laboratories

    06 8Aurolife Pharma LLC

    07 2Bionpharma

    08 3COMMAVE THERAP

    09 8ENDO OPERATIONS

    10 7Impax Laboratories

    11 6Intellipharmaceutics Corporation

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    13 2Neolpharma

    14 3Novel Laboratories, Inc.

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    Granules India Limited

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

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

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    Approval Date : 2020-09-09

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

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    Granules India Limited

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    Granules India Limited

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    Granules India Limited

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    Granules India Limited

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    Intellipharmaceutics Corporation

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    Dosage Strength : 5MG

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    Approval Date : 2021-11-23

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    Intellipharmaceutics Corporation

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    Approval Date : 2021-11-23

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    Intellipharmaceutics Corporation

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    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2013-11-18

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    Intellipharmaceutics Corporation

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    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2013-11-18

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    Sandoz B2B

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    Brand Name : FOCALIN

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    Approval Date : 2001-11-13

    Application Number : 21278

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    Approval Date : 2001-11-13

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    Dosage Strength : 10MG

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    Approval Date : 2001-11-13

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    Brand Name : FOCALIN XR

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    Approval Date : 2005-05-26

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    Approval Date : 2005-05-26

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    Brand Name : FOCALIN XR

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    Dosage Strength : 15MG

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    Approval Date : 2006-08-01

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    Brand Name : FOCALIN XR

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    Dosage Strength : 30MG

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    Approval Date : 2009-10-23

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    Brand Name : FOCALIN XR

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    Dosage Strength : 40MG

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    Approval Date : 2010-08-11

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    Brand Name : FOCALIN XR

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    Dosage Strength : 35MG

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    Approval Date : 2011-04-21

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    Brand Name : FOCALIN XR

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    Dosage Strength : 25MG

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    Approval Date : 2011-04-21

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2007-01-29

    Application Number : 77107

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2007-01-29

    Application Number : 77107

    Regulatory Info : DISCN

    Registration Country : USA

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

    Packaging :

    Approval Date : 2007-01-29

    Application Number : 77107

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : RX

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2013-11-19

    Application Number : 78908

    Regulatory Info : RX

    Registration Country : USA

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    Regulatory Info : RX

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2013-11-19

    Application Number : 78908

    Regulatory Info : RX

    Registration Country : USA

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    29

    Teva Pharmaceutical Industries

    Israel
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    Teva Pharmaceutical Industries

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2013-11-19

    Application Number : 78908

    Regulatory Info : RX

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    • EDQM
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    Regulatory Info : RX

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    DEXMETHYLPHENIDATE HYDROCHLORIDE

    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2014-05-19

    Application Number : 78908

    Regulatory Info : RX

    Registration Country : USA

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