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01 1Dr. Reddy's Laboratories

02 1Supriya Lifescience

03 2AFT Pharmaceuticals

04 4Accord healthcare

05 1Apotex Inc

06 1Aspiro Pharma

07 1Aurobindo Pharma Limited

08 1Baxter Healthcare Corporation

09 2Biological E

10 1Chia Tai Tianqing Pharmaceutical Group

11 1Cipla Medpro South Africa

12 1Etico Lifesciences

13 1Fresenius Kabi USA

14 1GENEYORK PHARMS

15 1Grupo Azevedos

16 1Hikma Pharmaceuticals

17 1JUNO PHARMACEUTICALS CORP.

18 1Juno Pharma SA (Pty) Ltd

19 1Lupin Ltd

20 1MERCK CANADA INC

21 2MSD INTL GMBH

22 1MSN Laboratories

23 2Medsurge Healthcare

24 7Merck & Co

25 1Naprod Life Sciences

26 1Navinta

27 1Piramal Enterprises Limited

28 1Polifarma

29 1Praxgen

30 1Qilu Pharmaceutical

31 2Reach Pharmaceuticals

32 1Sagent Pharmaceuticals

33 1Sakar Healthcare

34 1Sandoz B2B

35 1Steriscience

36 1Tarbis Farma Sl

37 2Tecnimede

38 1Teva Pharmaceutical Industries

39 1TherDose Pharma

40 2Viatris

41 1Zentiva

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

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 : 2020-12-09

Application Number : 211160

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info :

Registration Country : India

Fosaprepitant

Brand Name :

Dosage Form : Injection

Dosage Strength : 150MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

03

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2020-08-26

Application Number : 204025

Regulatory Info : DISCN

Registration Country : USA

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04

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2019-09-05

Application Number : 205020

Regulatory Info : DISCN

Registration Country : USA

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05

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2021-01-12

Application Number : 210625

Regulatory Info : RX

Registration Country : USA

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06

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2019-09-05

Application Number : 211860

Regulatory Info : RX

Registration Country : USA

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07

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2019-09-05

Application Number : 212309

Regulatory Info : RX

Registration Country : USA

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08

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2021-03-03

Application Number : 212143

Regulatory Info : RX

Registration Country : USA

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09

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2016-06-09

Application Number : 206197

Regulatory Info : RX

Registration Country : USA

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10

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2019-09-05

Application Number : 210689

Regulatory Info : RX

Registration Country : USA

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11

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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**

Packaging :

Approval Date : 2008-01-25

Application Number : 22023

Regulatory Info : DISCN

Registration Country : USA

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12

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : UNKNOWN

Dosage Strength : UNKNOWN

Packaging :

Approval Date :

Application Number : 204845

Regulatory Info :

Registration Country : USA

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16

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

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
Aus. Peptide Conference
Not Confirmed
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GENEYORK PHARMS

Country
arrow
Aus. Peptide Conference
Not Confirmed

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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