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    01 8Granules India Limited

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    Approval Date : 2021-11-23

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    Approval Date : 2013-11-18

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    Sandoz B2B

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    Approval Date : 2001-11-13

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    Sandoz B2B

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    Approval Date : 2009-10-23

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    Brand Name : FOCALIN XR

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    Approval Date : 2010-08-11

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    Brand Name : FOCALIN XR

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 35MG

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    Approval Date : 2011-04-21

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    Brand Name : FOCALIN XR

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    Approval Date : 2011-04-21

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    Teva Pharmaceutical Industries

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    Brand Name : DEXMETHYLPHENIDATE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2007-01-29

    Application Number : 77107

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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

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    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

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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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    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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    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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