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01 1Atidarsagen Autotemcel
02 1Atidarsagene Autotemcel
03 1Atidarsagene autotemcel
04 27Burosumab
05 1CD34+ Cell-Enriched Population Transduced with Lentiviral Vector Encoding Human Arylsulfatase A Gene, Autologous Human
06 1Droperidol
07 6Fentanyl
08 1Fentanyl Citrate
09 1Granisetron
10 1Iron
11 4Mitomycin
12 5Mogamulizumab
13 1Mogamulizumabum
14 1Nitroglycerin
15 1Testosterone
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01 1Concentrate For Infusion Solution
02 5Concentrate For Solution For Infusion
03 1Dispersion For Infusion
04 1Dispersion For Perfusion
05 1Fentanyl 100Mcg 10 Units Sublingual Use
06 1Fentanyl 200Mcg 10 Units Sublingual Use
07 1Fentanyl 300Mcg 10 Units Sublingual Use
08 1Fentanyl 400Mcg 10 Units Sublingual Use
09 1Fentanyl 600Mcg 10 Units Sublingual Use
10 1Fentanyl 800Mcg 10 Units Sublingual Use
11 1Granisetrone 3,1Mg 1 Unit Transdermal Use
12 2Infusion Solution
13 7Injectable Solution
14 3Injectable Solution In Pre-Filled Syringe
15 3Injection Solution
16 1Mitomycin 10Mg 1 Unit Parenteral Use
17 1Mitomycin 40Mg 1 Unit Parenteral Use
18 1Oral Solution
19 17Solution For Injection
20 1Sublingual Tablet
21 2Blank
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01 11 transdermal patch 3.1 mg/24 die
02 11 vial EV 10 mg
03 11 vial EV 40 mg
04 110 cpr subling 100 mcg
05 110 cpr subling 200 mcg
06 110 cpr subling 300 mcg
07 110 cpr subling 400 mcg
08 110 cpr subling 600 mcg
09 110 cpr subling 800 mcg
10 210MG
11 510mg
12 210mg/ml
13 11mg/ml
14 12-10millioncells/ml
15 12.5mg/ml
16 220MG
17 520mg
18 220mg/ml
19 230MG
20 530mg
21 230mg/ml
22 14MG
23 14mg/5ml
24 34mg/ml
25 150mcg
26 15ML
27 1Gel 60 G 2%
28 1Ung Rett 30 G 4 Mg/G
29 5Blank
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01 8Denmark
02 5Estonia
03 11Italy
04 1Malta
05 4Norway
06 8Spain
07 12Sweden
08 4Switzerland
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01 7Abstral
02 27Crysvita
03 1Dridol
04 3Libmeldy
05 1Libmeldy 2-
06 2Mitomycin
07 2Mitomycin C
08 6Poteligeo
09 1Rectogesic
10 1Sancuso
11 1Sytron
12 1Tostrex
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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injectable Solution
Dosage Strength : 10mg
Packaging :
Brand Name : Crysvita
Approval Date : 19/02/2018
Application Number : 20161206000011
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Dosage Strength : 10mg
Packaging :
Brand Name : Crysvita
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Dosage Strength : 20mg
Packaging :
Brand Name : Crysvita
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Dosage Strength : 30mg
Packaging :
Brand Name : Crysvita
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Brand Name : Crysvita
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Dispersion For Infusion
Dosage Strength :
Packaging :
Brand Name : Libmeldy
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Dispersion For Perfusion
Dosage Strength :
Packaging :
Brand Name : Libmeldy 2-
Approval Date : 19-10-2021
Application Number : 1201493001
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Infusion Solution
Dosage Strength :
Packaging :
Brand Name : Libmeldy
Approval Date : 17-12-2020
Application Number : 28106364519
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Injection Solution
Dosage Strength : 30mg
Packaging :
Brand Name : Crysvita
Approval Date : 19-02-2018
Application Number : 28105882316
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Solution For Injection
Dosage Strength : 30mg
Packaging :
Brand Name : Crysvita
Approval Date : 30-11-2023
Application Number : 28107068123
Regulatory Info : Prescription
Registration Country : Denmark

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