Synopsis
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EU WC
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NDC API
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USP
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DRUG PRODUCT COMPOSITIONS
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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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RLD :
TE Code :
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 37.5 IU/VIAL
Approval Date :
Application Number : 20378
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 1,050 IU/VIAL
Approval Date :
Application Number : 20378
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 450 IU/VIAL
Approval Date :
Application Number : 20378
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : GONAL-F RFF REDI-JECT
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 300 IU/0.5ML
Approval Date :
Application Number : 21684
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : GONAL-F RFF
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 75 IU/VIAL
Approval Date :
Application Number : 21765
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : GONAL-F
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 150 IU/VIAL
Approval Date :
Application Number : 21765
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : FOLLISTIM
Dosage Form : INJECTABLE;INTRAMUSCULAR, SUBCUTANEOUS
Dosage Strength : 75 IU/VIAL
Approval Date :
Application Number : 20582
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : FOLLISTIM AQ
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 75 IU/0.5ML
Approval Date :
Application Number : 21273
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : FOLLISTIM AQ
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 150 IU/0.5ML
Approval Date :
Application Number : 21273
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : FOLLISTIM AQ
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 150 IU/0.18ML
Approval Date :
Application Number : 21211
RX/OTC/DISCN :
RLD :
TE Code :

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Bemfola
Dosage Form : Solution For Injection
Dosage Strength : 225IU/0.375ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info :
Registration Country : Moldova
Brand Name : Rekovelle®
Dosage Form : Solution For Injection
Dosage Strength : 72mcg/2.16ml
Packaging :
Approval Date : 10-09-2020
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Rekovelle
Dosage Form : Solution For Injection
Dosage Strength : 36mcg/1.08ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Rekovelle
Dosage Form : Injectable Solution
Dosage Strength : 12MCG
Packaging :
Approval Date : 08-03-2017
Application Number : 1161150001
Regulatory Info : Cancelled
Registration Country : Spain

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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Puregon
Dosage Form : Injectable Solution
Dosage Strength : 50IU/0.5ml
Packaging :
Approval Date : 26/04/1999
Application Number : 19990426000013
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Gonal-F
Dosage Form : Solution For Injection
Dosage Strength : 450IU/0.72ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Estonia
Follitropin alfa; Lutropin alfa
Brand Name : Pergoveris
Dosage Form : Solution For Injection
Dosage Strength : 900IU/1.44ml; 450IU/1.44ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Gonal-f PEN UI
Dosage Form : Solution For Injection
Dosage Strength : 300IU/0.48ml
Packaging :
Approval Date : 20/04/2004
Application Number : 56689
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Puregon
Dosage Form : Solution For Injection
Dosage Strength : 150IU/0.18ml
Packaging :
Approval Date : 02/08/2004
Application Number : 20041118000050
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Puregon
Dosage Form : Injectable Solution
Dosage Strength : 900IU
Packaging :
Approval Date : 05-11-2004
Application Number : 96008041
Regulatory Info : Authorized
Registration Country : Spain

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