NanoAlvand is the entrance to Global Markets as a trusted Highly Potent Products manufacturer.

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01 4NanoAlvand
02 3Apotex Inc
03 1Incyte Biosciences Distribution
04 11Incyte Corporation
05 54Novartis Pharmaceuticals Corporation
06 3Novartis South Africa (Pty) Ltd
07 2ORIFARM GROUP AS
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01 1CREAM
02 1CREAM;TOPICAL
03 5Cream
04 3Oral Solution
05 1Syrup
06 3TAB
07 4TABLET
08 3TABLET; ORAL
09 5TABLET;ORAL
10 30Tablet
11 22Blank
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01 6Allowed
02 6Approved
03 6Authorized
04 5Marketed
05 2Not Marketed
06 3Originator
07 15Prescription
08 6RX
09 29Blank
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01 5JAKAFI
02 4JAKAVI
03 4Jackavi
04 44Jakavi
05 1Jakavi 15 mg
06 1Jakavi 20 mg
07 1Jakavi 5 mg
08 2OPZELURA
09 4Opzelura
10 1Opzelura g
11 4Relata
12 3Ruxolitinib
13 4Strong
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01 22Australia
02 5Canada
03 5Denmark
04 5Estonia
05 4Iran
06 7Norway
07 3South Africa
08 6Spain
09 6Sweden
10 6Switzerland
11 9USA
Regulatory Info :
Registration Country : Iran
Brand Name : Relata
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info :
Registration Country : Iran
Brand Name : Relata
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info :
Registration Country : Iran
Brand Name : Relata
Dosage Form : Tablet
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info :
Registration Country : Iran
Brand Name : Relata
Dosage Form : Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
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Regulatory Info :
Registration Country : USA
Brand Name : Ruxolitinib
Dosage Form : TABLET; ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 219660
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : Ruxolitinib
Dosage Form : TABLET; ORAL
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number : 219660
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : Ruxolitinib
Dosage Form : TABLET; ORAL
Dosage Strength : 2MG
Packaging :
Approval Date :
Application Number : 219660
Regulatory Info :
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : JAKAFI
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : JAKAFI
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : JAKAFI
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 15MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : JAKAFI
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 20MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : JAKAFI
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE
Packaging :
Approval Date : 2011-11-16
Application Number : 202192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : OPZELURA
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 1.5% BASE
Packaging :
Approval Date : 2021-09-21
Application Number : 215309
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Opzelura g
Dosage Form : Cream
Dosage Strength : 15mg
Packaging :
Approval Date : 30/01/2025
Application Number : 69443
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Jakavi
Dosage Form : Tablet
Dosage Strength : 5mg
Packaging :
Approval Date : 27/12/2012
Application Number : 62126
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Jakavi
Dosage Form : Tablet
Dosage Strength : 15mg
Packaging :
Approval Date : 27/12/2012
Application Number : 62126
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Jakavi
Dosage Form : Tablet
Dosage Strength : 20mg
Packaging :
Approval Date : 27/12/2012
Application Number : 62126
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Jakavi
Dosage Form : Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 27/12/2012
Application Number : 62126
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Jakavi
Dosage Form : Oral Solution
Dosage Strength : 5mg/ml
Packaging :
Approval Date : 27/03/2025
Application Number : 69722
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Jakavi
Dosage Form : Tablet
Dosage Strength : 10mg
Packaging :
Approval Date : 03/10/2014
Application Number : 20140311000017
Regulatory Info : Approved
Registration Country : Sweden
