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    01 3Dr. Reddy's Laboratories

    02 1Taro Pharmaceutical Industries

    03 2Adcock Ingram

    04 1American Regent

    05 3Amneal Pharmaceuticals

    06 2Apotex Inc

    07 3Aurobindo Pharma Limited

    08 1Barr Laboratories

    09 3Baxter Healthcare Corporation

    10 3Bionpharma

    11 2Bluefish Pharmaceuticals AB

    12 1Chartwell Pharmaceuticals llc

    13 2Epic Pharma. LLC.

    14 10F. Hoffmann-La Roche

    15 4Farbe Firma

    16 2Flagship Biotech International Pvt. Ltd

    17 1Fresenius Kabi AB Brunna

    18 3Fresenius Kabi USA

    19 1Ha Noi CPC1 Pharmaceutical JSC

    20 1Hameln Pharma GmbH

    21 7Hikma Pharmaceuticals

    22 1Igenius Life Sciences

    23 1Intra-Sana Laboratories

    24 1JAMP PHARMA

    25 3NORVIUM BIOSCIENCE

    26 2Natco Pharma

    27 1Natco Pharma (Canada) Inc

    28 1Omega Laboratories Limited

    29 1OrBion Pharmaceuticals

    30 2Pluviaendo

    31 2Rising Pharmaceuticals Inc

    32 2STADA Arzneimittel

    33 6Sandoz B2B

    34 2Teva Pharmaceutical Industries

    35 4Viatris

    36 3Wockhardt

    37 4XYZ Pharma

    38 1Yangtze River Pharmaceutical Group

    39 3Yung Shin Pharmaceutical Industrial

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    01

    Dr. Reddy's Laboratories

    India
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE PRESERVATIVE FREE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2007-12-31

    Application Number : 77165

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Dr. Reddy's Laboratories

    India
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    CPhI India 2024
    Booth #RH.E02
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    Regulatory Info : RX

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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

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    Approval Date : 2008-06-30

    Application Number : 77297

    Regulatory Info : RX

    Registration Country : USA

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    03

    Dr. Reddy's Laboratories

    India
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    Booth #RH.E02
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    Regulatory Info : RX

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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

    Packaging :

    Approval Date : 2007-12-31

    Application Number : 78392

    Regulatory Info : RX

    Registration Country : USA

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    04

    Taro Pharmaceutical Industries

    U.S.A
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    Regulatory Info : RX

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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

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    Approval Date : 2010-05-28

    Application Number : 90817

    Regulatory Info : RX

    Registration Country : USA

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    05

    Chartwell Pharmaceuticals llc

    U.S.A
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    Chartwell Pharmaceuticals llc

    U.S.A
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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 2008-02-27

    Application Number : 78037

    Regulatory Info : RX

    Registration Country : USA

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    06

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

    Switzerland
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    Regulatory Info : DISCN

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    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 3MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1993-12-29

    Application Number : 20239

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    F. Hoffmann-La Roche

    Switzerland
    The Pharmacy Technology
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    F. Hoffmann-La Roche

    Switzerland
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    The Pharmacy Technology
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    Regulatory Info : DISCN

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    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1994-03-11

    Application Number : 20239

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    F. Hoffmann-La Roche

    Switzerland
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    Regulatory Info : DISCN

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    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2004-09-17

    Application Number : 20239

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    F. Hoffmann-La Roche

    Switzerland
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    F. Hoffmann-La Roche

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    The Pharmacy Technology
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    Regulatory Info : DISCN

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    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1994-03-11

    Application Number : 20239

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    F. Hoffmann-La Roche

    Switzerland
    The Pharmacy Technology
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    The Pharmacy Technology
    Not Confirmed
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    Regulatory Info : DISCN

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    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1995-03-16

    Application Number : 20305

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    F. Hoffmann-La Roche

    Switzerland
    The Pharmacy Technology
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    The Pharmacy Technology
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    Regulatory Info : DISCN

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1998-06-15

    Application Number : 20305

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    F. Hoffmann-La Roche

    Switzerland
    The Pharmacy Technology
    Not Confirmed
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    F. Hoffmann-La Roche

    Switzerland
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    The Pharmacy Technology
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    Regulatory Info : DISCN

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : KYTRIL

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 2MG BASE/10ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2001-06-27

    Application Number : 21238

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Fresenius Kabi USA

    U.S.A
    The Pharmacy Technology
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    The Pharmacy Technology
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    Regulatory Info : RX

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2008-06-30

    Application Number : 78090

    Regulatory Info : RX

    Registration Country : USA

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    14

    Hikma Pharmaceuticals

    United Kingdom
    The Pharmacy Technology
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    The Pharmacy Technology
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    Regulatory Info : RX

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2007-12-31

    Application Number : 77177

    Regulatory Info : RX

    Registration Country : USA

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    15

    Hikma Pharmaceuticals

    United Kingdom
    The Pharmacy Technology
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    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : RX

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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG BASE/4ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2008-06-30

    Application Number : 77186

    Regulatory Info : RX

    Registration Country : USA

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    16

    Hikma Pharmaceuticals

    United Kingdom
    The Pharmacy Technology
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2008-06-30

    Application Number : 77187

    Regulatory Info : RX

    Registration Country : USA

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    17

    Hikma Pharmaceuticals

    United Kingdom
    The Pharmacy Technology
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    The Pharmacy Technology
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    Regulatory Info : DISCN

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 2007-12-31

    Application Number : 77842

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Hikma Pharmaceuticals

    United Kingdom
    The Pharmacy Technology
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    The Pharmacy Technology
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    Regulatory Info : RX

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML)

    Packaging :

    Approval Date : 2008-06-26

    Application Number : 77913

    Regulatory Info : RX

    Registration Country : USA

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    19

    Teva Pharmaceutical Industries

    Israel
    The Pharmacy Technology
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    The Pharmacy Technology
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    Regulatory Info : DISCN

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML (EQ 1MG BASE/ML)

    Packaging :

    Approval Date : 2008-01-03

    Application Number : 77963

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Teva Pharmaceutical Industries

    Israel
    The Pharmacy Technology
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    The Pharmacy Technology
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    GRANISETRON HYDROCHLORIDE

    Brand Name : GRANISETRON HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 2007-12-31

    Application Number : 78080

    Regulatory Info : DISCN

    Registration Country : USA

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