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

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01 1Dr. Reddy's Laboratories
02 1Supriya Lifescience
03 1Naprod Life Sciences
04 2AFT Pharmaceuticals
05 5Accord healthcare
06 1Apotex Inc
07 1Aspiro Pharma
08 1Aurobindo Pharma Limited
09 1Baxter Healthcare Corporation
10 2Biological E
11 1Caplin Point Laboratories Limited
12 1Chia Tai Tianqing Pharmaceutical Group
13 1Cipla Medpro South Africa
14 1Clinigen Group
15 1Etico Lifesciences
16 1Fresenius Kabi USA
17 1GENEYORK PHARMS
18 1Grupo Azevedos
19 1Hetero Drugs
20 1Hikma Pharmaceuticals
21 2Juno Pharmaceuticals Pty Ltd
22 1Lupin Ltd
23 1MERCK CANADA INC
24 1MSN Laboratories
25 2Medsurge Healthcare
26 10Merck & Co
27 1Navinta
28 1Piramal Enterprises Limited
29 1Polifarma
30 1Praxgen
31 1Qilu Pharmaceutical
32 2Reach Pharmaceuticals
33 1Sagent Pharmaceuticals
34 1Sakar Healthcare
35 1Steriscience
36 1Tarbis Farma Sl
37 2Tecnimede
38 1Teva Pharmaceutical Industries
39 1TherDose Pharma
40 2Viatris
41 1Zentiva
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01 1Fosaprepitant 150Mg 10 Ml 1 Units Parenteral Use
02 4INF
03 2INJ
04 3Injection
05 1Lyophilised Injection
06 1Lyophilized Injection
07 2POWDER FOR SOLUTION
08 22POWDER;INTRAVENOUS
09 3Powder For Infusion Solution
10 5Powder For Solution For Infusion
11 1Powder for Solution for Injection
12 1Powder for solution for Infusion
13 1Powder for solution for infusion
14 1SOLUTION;INTRAVENOUS
15 5Solution For Injection
16 1UNKNOWN
17 1Vial
18 6Blank
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01 2Approved
02 6Authorized
03 10DISCN
04 1Deregistered
05 5Generic
06 2Marketed
07 1Originator
08 2PRESCRIPTION
09 2Prescription
10 13RX
11 17Blank
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01 2EMEND
02 1EMEND IV
03 1EMETEND 150 mg
04 1Easan
05 1FOCINVEZ
06 21FOSAPREPITANT DIMEGLUMINE
07 1FOSAPREPITANT FOR INJECTION
08 2FOSAPREPITANT MEDSURGE
09 2FOSAPREPITANT MSN
10 2FOSAPREPITANT-AFT
11 1Fefprip
12 3Fosaprepitant Accord
13 1Fosaprepitant Cipla
14 1Fosaprepitant Equity
15 1Fosaprepitant Hikma
16 1Fosaprepitant Tarbis
17 1Fosaprepitant Tecnigen
18 1Fosaprepitant Zentiva
19 1IVEMEND 150 mg
20 1Item
21 6Ivemend
22 9Blank
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01 6Australia
02 2Canada
03 1Denmark
04 1Estonia
05 6India
06 1Italy
07 2Norway
08 2Portugal
09 6South Africa
10 6Spain
11 3Sweden
12 1Turkey
13 24USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 150MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Naprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Lyophilised Injection
Dosage Strength : 150MG/Vial
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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 : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info :
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
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

Regulatory Info : DISCN
Registration Country : USA
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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