Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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Canada
DRUG PRODUCT COMPOSITIONS
Regulatory FDF Prices
NA
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers

API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 10,000U/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; MULTIDOSE
Dosage Strength : 20,000U/2ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; MULTIDOSE
Dosage Strength : 20,000/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 2,000U/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 3,000U/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 40,000U/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 4,000U/ML
Packaging :
Approval Date :
Application Number : 103234
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2,000UNITS/ML
Packaging :
Approval Date :
Application Number : 125545
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 3,000UNITS/ML
Packaging :
Approval Date :
Application Number : 125545
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4,000UNITS/ML
Packaging :
Approval Date :
Application Number : 125545
Regulatory Info :
Registration Country : USA

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 10,000U/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; MULTIDOSE
Dosage Strength : 20,000U/2ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; MULTIDOSE
Dosage Strength : 20,000/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 2,000U/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 3,000U/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 40,000U/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : EPOGEN/PROCRIT
Dosage Form : VIAL; SINGLE-USE
Dosage Strength : 4,000U/ML
Approval Date :
Application Number : 103234
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 2,000UNITS/ML
Approval Date :
Application Number : 125545
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4,000UNITS/ML
Approval Date :
Application Number : 125545
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : RETACRIT
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10,000UNITS/ML
Approval Date :
Application Number : 125545
RX/OTC/DISCN :
RLD :
TE Code :

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eprex
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 4000IU
Packaging :
Approval Date : 1995-05-01
Application Number : 60582
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Retacrit
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 4000IU
Packaging :
Approval Date : 2008-02-27
Application Number : 07431008
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eporatio
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 10000IU
Packaging :
Approval Date : 2009-11-25
Application Number : 09573015
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eporatio
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 3000IU
Packaging :
Approval Date : 2015-06-24
Application Number : 109573031
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eporatio
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 2000IU
Packaging :
Approval Date : 2009-11-25
Application Number : 09573004
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Eporatio
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 2000IU
Packaging :
Approval Date : 2009-11-25
Application Number : 09573003
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Binocrit
Dosage Form : Injectable In Pre-Filled Syringe
Dosage Strength : 30000IU
Packaging :
Approval Date : 2009-12-22
Application Number : 07410024
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Binocrit,
Dosage Form : Injectable Solution In A Pre-Filled Syringe
Dosage Strength : 10000IU
Packaging :
Approval Date : 2008-02-18
Application Number : 07410016
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Binocrit,
Dosage Form : Injectable Solution In A Pre-Filled Syringe
Dosage Strength : 6000IU
Packaging :
Approval Date : 2008-02-18
Application Number : 07410012
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Binocrit
Dosage Form : Injectable Solution In A Pre-Filled Syringe
Dosage Strength : 40000IU
Packaging :
Approval Date : 2011-03-23
Application Number : 07410051
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info :
Registration Country : Thailand
RECOMBINANT HUMAN ERYTHROPOIETIN
Brand Name : Hema-Plus
Dosage Form : Solution For Injection
Dosage Strength : 4000IU/1ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Thailand

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Packaging :
Regulatory Info :
RECOMBINANT HUMAN ERYTHROPOIETIN
Dosage : Solution For Injection
Dosage Strength : 4000IU/1ML
Brand Name : Hema-Plus
Approval Date :
Application Number :
Registration Country : Thailand

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