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    Approval Date : 1998-04-13

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    ANI Pharmaceuticals Inc

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    Approval Date : 1996-05-16

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    ANI Pharmaceuticals Inc

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    Brand Name : MEXILETINE HYDROCHLORIDE

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    Dosage Strength : 250MG

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    Approval Date : 1996-05-16

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    Boehringer Ingelheim GmbH

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    Brand Name : MEXITIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-12-30

    Application Number : 18873

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    Boehringer Ingelheim GmbH

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    Brand Name : MEXITIL

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-12-30

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    Boehringer Ingelheim GmbH

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    Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1985-12-30

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    Novast Laboratories

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    Dosage Strength : 150MG

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    Approval Date : 2021-01-25

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    Dosage Strength : 200MG

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    Approval Date : 2021-01-25

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    Novast Laboratories

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    Approval Date : 2021-01-25

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    Rising Pharmaceuticals Inc

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    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

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    Approval Date : 2022-08-26

    Application Number : 215315

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    Rising Pharmaceuticals Inc

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    Brand Name : MEXILETINE HYDROCHLORIDE

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    Dosage Strength : 200MG

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    Approval Date : 2022-08-26

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    Rising Pharmaceuticals Inc

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    Dosage Strength : 250MG

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    Approval Date : 2022-08-26

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    Senores Pharmaceuticals

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    Brand Name : MEXILETINE HYDROCHLORIDE

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    Dosage Strength : 150MG

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    Approval Date : 2021-10-01

    Application Number : 214089

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    Senores Pharmaceuticals

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    Brand Name : MEXILETINE HYDROCHLORIDE

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    Dosage Strength : 200MG

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    Approval Date : 2021-10-01

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    Senores Pharmaceuticals

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    Brand Name : MEXILETINE HYDROCHLORIDE

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    Dosage Strength : 250MG

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    Approval Date : 2021-10-01

    Application Number : 214089

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    Teva Pharmaceutical Industries

    Israel
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    Teva Pharmaceutical Industries

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Packaging :

    Approval Date : 1995-05-16

    Application Number : 74377

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    Teva Pharmaceutical Industries

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    Regulatory Info : RX

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 1995-05-16

    Application Number : 74377

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    Teva Pharmaceutical Industries

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    Regulatory Info : RX

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 1995-05-16

    Application Number : 74377

    Regulatory Info : RX

    Registration Country : USA

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Packaging :

    Approval Date : 2020-07-22

    Application Number : 213500

    Regulatory Info : RX

    Registration Country : USA

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2020-07-22

    Application Number : 213500

    Regulatory Info : RX

    Registration Country : USA

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    CROSSMEDIKA SA

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 2020-07-22

    Application Number : 213500

    Regulatory Info : RX

    Registration Country : USA

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