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    Dr. Reddy's Laboratories

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    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

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    Approval Date : 2002-07-03

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    Dr. Reddy's Laboratories

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    ANI Pharmaceuticals Inc

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    Approval Date : 2002-07-12

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    ANI Pharmaceuticals Inc

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    ANI Pharmaceuticals Inc

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    Approval Date : 2002-07-03

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    ANI Pharmaceuticals Inc

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    ANI Pharmaceuticals Inc

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    Approval Date : 2004-09-30

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    ANI Pharmaceuticals Inc

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    Approval Date : 2004-09-30

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    ANI Pharmaceuticals Inc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

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    Approval Date : 2003-04-09

    Application Number : 76371

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    10

    ANI Pharmaceuticals Inc

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    ANI Pharmaceuticals Inc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

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    Dosage Strength : EQ 4MG BASE

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    Approval Date : 2003-04-09

    Application Number : 76371

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Apotex Inc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 2004-01-16

    Application Number : 76533

    Regulatory Info : RX

    Registration Country : USA

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    12

    Apotex Inc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2004-01-16

    Application Number : 76533

    Regulatory Info : RX

    Registration Country : USA

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    13

    Apotex Inc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 2MG BASE

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    Approval Date : 2012-02-03

    Application Number : 78868

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    Aurobindo Pharma Limited

    India
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    Approval Date : 2003-12-16

    Application Number : 76282

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    Aurobindo Pharma Limited

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    Brand Name : TIZANIDINE HYDROCHLORIDE

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    Dosage Strength : EQ 4MG BASE

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    Approval Date : 2003-12-16

    Application Number : 76282

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    16

    Chartwell Pharmaceuticals llc

    U.S.A
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    Brand Name : TIZANIDINE HYDROCHLORIDE

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    Dosage Strength : EQ 2MG BASE

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    Approval Date : 2002-11-26

    Application Number : 76280

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    Chartwell Pharmaceuticals llc

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    Brand Name : TIZANIDINE HYDROCHLORIDE

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    Dosage Strength : EQ 4MG BASE

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    Approval Date : 2002-06-27

    Application Number : 76280

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    18

    Epic Pharma. LLC.

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

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    Approval Date : 2002-10-11

    Application Number : 76347

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    Registration Country : USA

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    Epic Pharma. LLC.

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    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

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    Approval Date : 2002-10-11

    Application Number : 76347

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    Registration Country : USA

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    Legacy Pharma

    Barbados
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    Brand Name : ZANAFLEX

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    Approval Date : 1996-11-27

    Application Number : 20397

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    Brand Name : ZANAFLEX

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    Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-02-04

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    Approval Date : 2002-08-29

    Application Number : 21447

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    TIZANIDINE HYDROCHLORIDE

    Brand Name : ZANAFLEX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2002-08-29

    Application Number : 21447

    Regulatory Info : RX

    Registration Country : USA

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    24

    Legacy Pharma

    Barbados
    Pharmtech & Ingredients
    Not Confirmed
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    Legacy Pharma

    Barbados
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    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : ZANAFLEX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 6MG BASE

    Packaging :

    Approval Date : 2002-08-29

    Application Number : 21447

    Regulatory Info : RX

    Registration Country : USA

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    25

    Oxford Pharm

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Oxford Pharm

    U.S.A
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    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 2003-10-20

    Application Number : 76281

    Regulatory Info : RX

    Registration Country : USA

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    26

    Oxford Pharm

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Oxford Pharm

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2003-10-20

    Application Number : 76281

    Regulatory Info : RX

    Registration Country : USA

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    27

    Rising Pharmaceuticals Inc

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 2003-03-28

    Application Number : 76354

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Rising Pharmaceuticals Inc

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2003-03-28

    Application Number : 76354

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Sun Pharmaceutical Industries Limit...

    India
    Pharmtech & Ingredients
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 2003-09-29

    Application Number : 76416

    Regulatory Info : RX

    Registration Country : USA

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    30

    Sun Pharmaceutical Industries Limit...

    India
    Pharmtech & Ingredients
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
    arrow
    Pharmtech & Ingredients
    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    TIZANIDINE HYDROCHLORIDE

    Brand Name : TIZANIDINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 4MG BASE

    Packaging :

    Approval Date : 2003-09-29

    Application Number : 76416

    Regulatory Info : RX

    Registration Country : USA

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