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    01

    Dr. Reddy's Laboratories

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    Tofacitinib Citrate

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    Breckenridge Pharmaceutical

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    03

    NanoAlvand

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    NanoAlvand

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    05

    Ajanta Pharma Limited

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    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB CITRATE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2021-06-01

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    Aurobindo Pharma Limited

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    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB

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    Dosage Strength : EQ 11MG BASE

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    Approval Date : 2024-06-03

    Application Number : 218462

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    Bluepharma

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    Bluepharma

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    09

    Dexcel Pharma

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    Brand Name : TOFACITINIB CITRATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 11MG BASE

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    Approval Date : 2024-12-16

    Application Number : 218668

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    Dexcel Pharma

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    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB CITRATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 22MG

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    11

    Hikma Pharmaceuticals

    United Kingdom
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    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB CITRATE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 2023-09-25

    Application Number : 216878

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    12

    Laboratorio Eczane Pharma

    Argentina
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    Tofacitinib

    Brand Name : Tofax

    Dosage Form : Tablet

    Dosage Strength : 5MG

    Packaging : 60/180 Tabs

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    Registration Country : Argentina

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    13

    Laboratorio Eczane Pharma

    Argentina
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    Laboratorio Eczane Pharma

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    Tofacitinib

    Brand Name : Tofax

    Dosage Form : Tablet

    Dosage Strength : 5MG

    Packaging : 60/180

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    Registration Country : Argentina

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    14

    Micro Labs Limited

    India
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    Micro Labs Limited

    India
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    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 2023-03-13

    Application Number : 209738

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    15

    MSN Laboratories

    India
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    MSN Laboratories

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    Brand Name : TOFACITINIB

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    Application Number : 217299

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    16

    MSN Laboratories

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    17

    Pfizer Inc

    U.S.A
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    Pfizer Inc

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    TOFACITINIB CITRATE

    Brand Name : XELJANZ

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 2012-11-06

    Application Number : 203214

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    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
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    Approval Date : 2018-05-30

    Application Number : 203214

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    19

    Pfizer Inc

    U.S.A
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    Pfizer Inc

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    Brand Name : XELJANZ XR

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 11MG BASE

    Packaging :

    Approval Date : 2016-02-23

    Application Number : 208246

    Regulatory Info : RX

    Registration Country : USA

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    20

    Pfizer Inc

    U.S.A
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    TOFACITINIB CITRATE

    Brand Name : XELJANZ XR

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 22MG BASE

    Packaging :

    Approval Date : 2019-12-12

    Application Number : 208246

    Regulatory Info : RX

    Registration Country : USA

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    21

    Pfizer Inc

    U.S.A
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    Brand Name : XELJANZ

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 1MG BASE/ML

    Packaging :

    Approval Date : 2020-09-25

    Application Number : 213082

    Regulatory Info : RX

    Registration Country : USA

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    22

    Prinston

    U.S.A
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    TOFACITINIB

    Brand Name : TOFACITINIB

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date :

    Application Number : 209923

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    Registration Country : USA

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    23

    Unichem Laboratories Limited

    India
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    Approval Date :

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    Regulatory Info : Generic

    Registration Country : India

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    Yaopharma

    China
    PharmScience R&D
    Not Confirmed
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    Yaopharma

    China
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    Tofacitinib

    Brand Name : Tofacitinib

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    Approval Date :

    Application Number : 215552

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    Registration Country : USA

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    25

    Yaopharma

    China
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    Tofacitinib

    Brand Name : Tofacitinib

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date :

    Application Number : 215552

    Regulatory Info :

    Registration Country : USA

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    Zydus Pharmaceuticals

    U.S.A
    PharmScience R&D
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    PharmScience R&D
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    Regulatory Info : DISCN

    Registration Country : USA

    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB CITRATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2023-03-13

    Application Number : 209829

    Regulatory Info : DISCN

    Registration Country : USA

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    Zydus Pharmaceuticals

    U.S.A
    PharmScience R&D
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 11MG BASE

    Packaging :

    Approval Date : 2021-08-19

    Application Number : 214264

    Regulatory Info : DISCN

    Registration Country : USA

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    Zydus Pharmaceuticals

    U.S.A
    PharmScience R&D
    Not Confirmed
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    Zydus Pharmaceuticals

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    TOFACITINIB CITRATE

    Brand Name : TOFACITINIB

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 22MG BASE

    Packaging :

    Approval Date : 2021-08-19

    Application Number : 214264

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    ANNORA PHARMA PRIVATE LIMITED

    Country
    PharmScience R&D
    Not Confirmed
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    ANNORA PHARMA PRIVATE LIMITED

    Country
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    Regulatory Info :

    Registration Country : USA

    TOFACITINIB

    Brand Name : TOFACITINIB

    Dosage Form : TABLET

    Dosage Strength : 10MG

    Packaging :

    Approval Date :

    Application Number : 218437

    Regulatory Info :

    Registration Country : USA

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    ANNORA PHARMA PRIVATE LIMITED

    Country
    PharmScience R&D
    Not Confirmed
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    ANNORA PHARMA PRIVATE LIMITED

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    Regulatory Info :

    Registration Country : USA

    TOFACITINIB

    Brand Name : TOFACITINIB

    Dosage Form : TABLET

    Dosage Strength : 5MG

    Packaging :

    Approval Date :

    Application Number : 218437

    Regulatory Info :

    Registration Country : USA

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