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    Mexiletine, HCl

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    Actavis Inc

    Ireland
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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

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    Approval Date : 1997-02-26

    Application Number : 74711

    Regulatory Info : DISCN

    Registration Country : USA

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

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    Approval Date : 1997-02-26

    Application Number : 74711

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

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    Approval Date : 1997-02-26

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

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    Approval Date : 1998-04-13

    Application Number : 74865

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    05

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

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    Approval Date : 1998-04-13

    Application Number : 74865

    Regulatory Info : DISCN

    Registration Country : USA

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

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    Approval Date : 1998-04-13

    Application Number : 74865

    Regulatory Info : DISCN

    Registration Country : USA

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    ANI Pharmaceuticals Inc

    U.S.A
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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Packaging :

    Approval Date : 1996-05-16

    Application Number : 74450

    Regulatory Info : RX

    Registration Country : USA

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    08

    ANI Pharmaceuticals Inc

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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 1996-05-16

    Application Number : 74450

    Regulatory Info : RX

    Registration Country : USA

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    09

    ANI Pharmaceuticals Inc

    U.S.A
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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 : 1996-05-16

    Application Number : 74450

    Regulatory Info : RX

    Registration Country : USA

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    10

    Boehringer Ingelheim GmbH

    Germany
    Health 2.0 Conference
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    MEXILETINE HYDROCHLORIDE

    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**

    Packaging :

    Approval Date : 1985-12-30

    Application Number : 18873

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Boehringer Ingelheim GmbH

    Germany
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    MEXILETINE HYDROCHLORIDE

    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**

    Packaging :

    Approval Date : 1985-12-30

    Application Number : 18873

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Boehringer Ingelheim GmbH

    Germany
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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXITIL

    Dosage Form : CAPSULE;ORAL

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

    Packaging :

    Approval Date : 1985-12-30

    Application Number : 18873

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Senores Pharmaceuticals

    India
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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Packaging :

    Approval Date : 2021-10-01

    Application Number : 214089

    Regulatory Info : RX

    Registration Country : USA

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    14

    Senores Pharmaceuticals

    India
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    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2021-10-01

    Application Number : 214089

    Regulatory Info : RX

    Registration Country : USA

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    15

    Teva Pharmaceutical Industries

    Israel
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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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    16

    Teva Pharmaceutical Industries

    Israel
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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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    17

    Teva Pharmaceutical Industries

    Israel
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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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    CROSSMEDIKA SA

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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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    19

    CROSSMEDIKA SA

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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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    20

    CROSSMEDIKA SA

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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 : 2020-07-22

    Application Number : 213500

    Regulatory Info : RX

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.