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    01 1Dr. Reddy's Laboratories

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    05 1Apotex Inc

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    01

    Dr. Reddy's Laboratories

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

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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2020-12-09

    Application Number : 211160

    Regulatory Info : RX

    Registration Country : USA

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    02

    Supriya Lifescience

    India
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    CPhI WW Frankfurt
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    Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

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    03

    Accord healthcare

    United Kingdom
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    Accord healthcare

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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2020-08-26

    Application Number : 204025

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Apotex Inc

    Canada
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2019-09-05

    Application Number : 205020

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Aurobindo Pharma Limited

    India
    Organic Process R&D
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    Aurobindo Pharma Limited

    India
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    Organic Process R&D
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2021-01-12

    Application Number : 210625

    Regulatory Info : RX

    Registration Country : USA

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    06

    Baxter Healthcare Corporation

    U.S.A
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2019-09-05

    Application Number : 211860

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    07

    Biological E

    India
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    Biological E

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    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2019-09-05

    Application Number : 212309

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    08

    Chia Tai Tianqing Pharmaceutical Gr...

    China
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    Chia Tai Tianqing Pharmaceutical Gr...

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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2021-03-03

    Application Number : 212143

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    09

    Fresenius Kabi USA

    U.S.A
    Organic Process R&D
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    Fresenius Kabi USA

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    Organic Process R&D
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2016-06-09

    Application Number : 206197

    Regulatory Info : RX

    Registration Country : USA

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    10

    Lupin Ltd

    India
    Organic Process R&D
    Not Confirmed
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    Lupin Ltd

    India
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    Organic Process R&D
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    Regulatory Info : RX

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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

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    Approval Date : 2019-09-05

    Application Number : 210689

    Regulatory Info : RX

    Registration Country : USA

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    11

    Merck & Co

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Merck & Co

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

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : EMEND

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 115MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2008-01-25

    Application Number : 22023

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Merck & Co

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Merck & Co

    U.S.A
    arrow
    Organic Process R&D
    Not Confirmed
    • fda
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    Regulatory Info : RX

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : EMEND

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2010-11-12

    Application Number : 22023

    Regulatory Info : RX

    Registration Country : USA

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    13

    MSN Laboratories

    India
    Organic Process R&D
    Not Confirmed
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    MSN Laboratories

    India
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    Organic Process R&D
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2019-09-05

    Application Number : 209965

    Regulatory Info : RX

    Registration Country : USA

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    14

    Navinta

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Navinta

    U.S.A
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    Organic Process R&D
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2020-08-20

    Application Number : 212957

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Sagent Pharmaceuticals

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    Organic Process R&D
    Not Confirmed
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    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : UNKNOWN

    Dosage Strength : UNKNOWN

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    Approval Date :

    Application Number : 204845

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    Registration Country : USA

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    16

    Sandoz B2B

    Switzerland
    Organic Process R&D
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    Organic Process R&D
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2020-12-08

    Application Number : 203939

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Teva Pharmaceutical Industries

    Israel
    Organic Process R&D
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Organic Process R&D
    Not Confirmed
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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2019-09-05

    Application Number : 210064

    Regulatory Info : RX

    Registration Country : USA

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    18

    Viatris

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Viatris

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

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    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 115MG BASE/VIAL

    Packaging :

    Approval Date : 2019-09-05

    Application Number : 204015

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Viatris

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Viatris

    U.S.A
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    Organic Process R&D
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2019-09-05

    Application Number : 204015

    Regulatory Info : RX

    Registration Country : USA

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    20

    GENEYORK PHARMS

    Country
    Organic Process R&D
    Not Confirmed
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    GENEYORK PHARMS

    Country
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    Organic Process R&D
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    FOSAPREPITANT DIMEGLUMINE

    Brand Name : FOSAPREPITANT DIMEGLUMINE

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 150MG BASE/VIAL

    Packaging :

    Approval Date : 2019-09-05

    Application Number : 211624

    Regulatory Info : DISCN

    Registration Country : USA

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