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 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 1Clinigen Group
13 1Etico Lifesciences
14 1Fresenius Kabi USA
15 1GENEYORK PHARMS
16 1Grupo Azevedos
17 1Hetero Drugs
18 1Hikma Pharmaceuticals
19 2Juno Pharmaceuticals Pty Ltd
20 1Lupin Ltd
21 1MERCK CANADA INC
22 2MSD INTL GMBH
23 1MSN Laboratories
24 2Medsurge Healthcare
25 7Merck & Co
26 1Naprod Life Sciences
27 1Navinta
28 1Piramal Enterprises Limited
29 1Polifarma
30 1Praxgen
31 1Qilu Pharmaceutical
32 2Reach Pharmaceuticals
33 1Sagent Pharmaceuticals
34 1Sakar Healthcare
35 1Sandoz B2B
36 1Steriscience
37 1Tarbis Farma Sl
38 2Tecnimede
39 1Teva Pharmaceutical Industries
40 1TherDose Pharma
41 2Viatris
42 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 1Powder 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 3Solution For Injection
16 1UNKNOWN
17 1Vial
18 8Blank
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01 2Approved
02 6Authorized
03 10DISCN
04 1Deregistered
05 5Generic
06 1Originator
07 2Prescription
08 13RX
09 19Blank
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01 2EMEND
02 1EMEND IV
03 1EMETEND 150 mg
04 1Easan
05 2Emend IV
06 1FOCINVEZ
07 21FOSAPREPITANT DIMEGLUMINE
08 1FOSAPREPITANT FOR INJECTION
09 2FOSAPREPITANT MEDSURGE
10 2FOSAPREPITANT MSN
11 2FOSAPREPITANT-AFT
12 1Fefprip
13 2Fosaprepitant Accord
14 1Fosaprepitant Cipla
15 1Fosaprepitant Equity
16 1Fosaprepitant Hikma
17 1Fosaprepitant Tarbis
18 1Fosaprepitant Tecnigen
19 1Fosaprepitant Zentiva
20 1IVEMEND 150 mg
21 1Item
22 3Ivemend
23 9Blank
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01 8Australia
02 2Canada
03 6India
04 1Italy
05 2Portugal
06 6South Africa
07 6Spain
08 3Sweden
09 1Turkey
10 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
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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 : 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 : DISCN
Registration Country : USA
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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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 : 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 : 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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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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