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    (+)-Mexiletine Hydrochloride

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    01 3ANI PHARMS

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    WATSON LABS

    Ireland
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    RLD : No

    TE Code :

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Approval Date : 1997-02-26

    Application Number : 74711

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    ANI PHARMS

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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Approval Date : 1996-05-16

    Application Number : 74450

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    ANI PHARMS

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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Approval Date : 1996-05-16

    Application Number : 74450

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    ANI PHARMS

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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

    Approval Date : 1996-05-16

    Application Number : 74450

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    BOEHRINGER INGELHEIM

    Germany
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    RLD : Yes

    TE Code :

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    Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1985-12-30

    Application Number : 18873

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    BOEHRINGER INGELHEIM

    Germany
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1985-12-30

    Application Number : 18873

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    07

    BOEHRINGER INGELHEIM

    Germany
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    RLD : Yes

    TE Code :

    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**

    Approval Date : 1985-12-30

    Application Number : 18873

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    TEVA

    Israel
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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 150MG

    Approval Date : 1995-05-16

    Application Number : 74377

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    TEVA

    Israel
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    TEVA

    Israel
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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 200MG

    Approval Date : 1995-05-16

    Application Number : 74377

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    TEVA

    Israel
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    TEVA

    Israel
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    RLD : No

    TE Code : AB

    MEXILETINE HYDROCHLORIDE

    Brand Name : MEXILETINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 250MG

    Approval Date : 1995-05-16

    Application Number : 74377

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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