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01 1Dr. Reddy's Laboratories

02 1Supriya Lifescience

03 1Naprod Life Sciences

04 2AFT Pharmaceuticals

05 1ARTHUR GRP

06 1Accord healthcare

07 1Apotex Inc

08 1Aspiro Pharma

09 1Aurobindo Pharma Limited

10 1Baxter Healthcare Corporation

11 2Biological E

12 1Chia Tai Tianqing Pharmaceutical Group

13 1Cipla Medpro South Africa

14 1Etico Lifesciences

15 1Fresenius Kabi USA

16 1GENEYORK PHARMS

17 1Grupo Azevedos

18 1Kahma Group

19 1Lupin Ltd

20 1MERCK CANADA INC

21 2MSD INTL GMBH

22 1MSN Laboratories

23 2Medsurge Healthcare

24 8Merck & Co

25 1Navinta

26 1Piramal Enterprises Limited

27 1Polifarma

28 1Qilu Pharmaceutical

29 2Reach Pharmaceuticals

30 1Sagent Pharmaceuticals

31 1Sakar Healthcare

32 1Sandoz B2B

33 1Steriscience

34 1Tecnimede

35 1Teva Pharmaceutical Industries

36 1TherDose Pharma

37 2Viatris

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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

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Fosaprepitant Dimeglumine

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 150MG/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2021-07-29

Application Number : 214616

Regulatory Info : RX

Registration Country : USA

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name :

Dosage Form : Lyophilized Injection

Dosage Strength : 150MG/ML

Packaging : Single dose glass vial

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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16

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

fosaprepitant dimeglumine

Brand Name : IVEMEND

Dosage Form : POWDER FOR SOLUTION FOR INFUSION

Dosage Strength : 150 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

fosaprepitant dimeglumine

Brand Name : IVEMEND

Dosage Form : POWDER FOR SOLUTION FOR INFUSION

Dosage Strength : 115 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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18

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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fosaprepitant

Brand Name : Ivemend

Dosage Form : Fosaprepitant 150Mg 10 Ml 1 Units Parenteral Use

Dosage Strength : 1 vial EV 10 ml 150 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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19

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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20

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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 : RX

Registration Country : USA

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21

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2023-05-16

Application Number : 214683

Regulatory Info : RX

Registration Country : USA

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22

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2020-09-08

Application Number : 213106

Regulatory Info : RX

Registration Country : USA

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23

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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24

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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25

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOCINVEZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/50ML (EQ 3MG BASE/ML)

Packaging :

Approval Date : 2023-08-22

Application Number : 216686

Regulatory Info : RX

Registration Country : USA

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26

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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27

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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28

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
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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29

GENEYORK PHARMS

Country
Pharmtech & Ingredients
Not Confirmed
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GENEYORK PHARMS

Country
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Pharmtech & Ingredients
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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30

ARTHUR GRP

Country
Pharmtech & Ingredients
Not Confirmed
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ARTHUR GRP

Country
arrow
Pharmtech & Ingredients
Not Confirmed

FOSAPREPITANT DIMEGLUMINE

Brand Name : FOSAPREPITANT DIMEGLUMINE

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 150MG BASE/VIAL

Packaging :

Approval Date : 2021-10-04

Application Number : 213199

Regulatory Info : DISCN

Registration Country : USA

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