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01 6PEMIGATINIB
02 15Pemigatinib
03 6Ponatinib
04 4Ponatinib hydrochloride
05 3Ponatinibhydroklorid
06 3Put It Away
07 1RETIFANLIMAB
08 1RETIFANLIMAB-DLWR
09 1RUXOLITINIB (RUXOLITINIB PHOSPHATE)
10 6RUXOLITINIB PHOSPHATE
11 2Retifanlimab
12 1Retifanlimab
13 2Ruxolitinib
14 2Ruxolitinib Phosphate
15 1TAFASITAMAB
16 4Tafasitamab
17 1Tafasitamabum
18 1axatilimab-csfr
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01 11INCYTE CORP
02 6INCYTE CORPORATION
03 18Incyte Biosciences Distribution B.V.
04 8Incyte Biosciences Distribution BV
05 8Incyte Biosciences Distribution Bv
06 9Incyte Biosciences International S?rl
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01 1CREAM
02 1CREAM;TOPICAL
03 2Concentrate For Solution For Infusion
04 4Cream
05 13Film Coated Tablet
06 3Film-Coated Tablet
07 2INJECTABLE;INTRAVENOUS
08 1Injectable Solution
09 1POWDER FOR SOLUTION
10 1Powder For Concentrate For Infusion Solution
11 3Powder For Concentrate For Solution For Infusion
12 1SOLUTION
13 1Solution For Injection
14 3TABLET
15 8TABLET;ORAL
16 15Tablet
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01 11.5%/W/W
02 313.5MG
03 313.5mg
04 1135mg
05 215MG
06 615mg
07 215mg/g
08 1200MG
09 1200MG/VIAL
10 4200mg
11 125MG/ML
12 130MG
13 430mg
14 34.5MG
15 34.5mg
16 140mg
17 145MG
18 445mg
19 150 MG/ML
20 1500MG/20ML(25MG/ML)
21 1500mg
22 2500mg/20ml
23 39MG
24 29mg
25 1EQ 1.5% BASE
26 1EQ 10MG BASE
27 1EQ 15MG BASE
28 1EQ 20MG BASE
29 1EQ 25MG BASE
30 1EQ 5MG BASE
31 2Blank
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01 6Canada
02 9Estonia
03 8Norway
04 8Spain
05 9Sweden
06 9Switzerland
07 11USA
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Regulatory Info :
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : NIKTIMVO
Dosage Strength : 50 MG/ML
Packaging :
Approval Date :
Application Number : 761411
Regulatory Info :
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PEMAZYRE
Dosage Strength : 4.5MG
Packaging :
Approval Date : 2020-04-17
Application Number : 213736
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PEMAZYRE
Dosage Strength : 9MG
Packaging :
Approval Date : 2020-04-17
Application Number : 213736
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PEMAZYRE
Dosage Strength : 13.5MG
Packaging :
Approval Date : 2020-04-17
Application Number : 213736
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Limited-Term
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength : 4.5mg
Packaging :
Approval Date : 13/07/2021
Application Number : 68143
Regulatory Info : Limited-Term
Registration Country : Switzerland

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Regulatory Info : Limited-Term
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength : 9mg
Packaging :
Approval Date : 13/07/2021
Application Number : 68143
Regulatory Info : Limited-Term
Registration Country : Switzerland

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Regulatory Info : Limited-Term
Registration Country : Switzerland
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength : 13.5mg
Packaging :
Approval Date : 13/07/2021
Application Number : 68143
Regulatory Info : Limited-Term
Registration Country : Switzerland

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength : 13.5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength : 4.5mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Tablet
Brand Name : Pemazyre
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
