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

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01 1NanoAlvand
02 2Campus Pharma AB
03 2Centocor
04 2Central Procurement & Supplies Unit
05 2Ebb Medical
06 2Farmatek
07 2GLAND PHARMA LIMITED
08 7GSK
09 6Janssen-Cilag
10 8Johnson & Johnson Innovative Medicine
11 2LABORATORIOS NORMON SA
12 2Meitheal Pharmaceuticals
13 2NTC
14 4Sun Pharmaceutical Industries Limited
15 2Viatris
16 1WELLCOME FOUNDATION LTD
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01 2Epoprostenol 0.5Mg 1 Unit Parenteral Use
02 3Epoprostenol 1,5Mg 1 Unit Parenteral Use
03 12INJECTABLE;INJECTION
04 2Lyophilized Powder for Injection
05 4POWDER FOR SOLUTION
06 6Powder And Solvent For Infusion Solution
07 5Powder For Infusion Solution
08 1Powder For Solution For Infusion
09 4Solution For Infusion
10 3Solution For Injection
11 5Blank
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01 2Allowed
02 2Authorised
03 5Authorized
04 2Cancelled
05 2DISCN
06 4Deregistered
07 5Prescription
08 10RX
09 2Suspended
10 1Withdrawn
11 12Blank
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01 2CARIPUL
02 2Caripul
03 8EPOPROSTENOL SODIUM
04 1Eponol®
05 2Epoprostenol
06 2Epoprostenol Campuspharma
07 2Epoprostenol Ebb
08 2Epoprostenol Normon
09 2Epoprostenol Sun
10 4FLOLAN
11 5Flolan
12 2VELETRI
13 11Veletri
14 2Blank
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01 4Australia
02 4Canada
03 1Estonia
04 1Iran
05 5Italy
06 3Malta
07 9Spain
08 4Sweden
09 2Switzerland
10 2Turkey
11 12USA
Regulatory Info :
Registration Country : Iran
Brand Name : Eponol®
Dosage Form :
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
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Regulatory Info :
Registration Country : Turkey
Brand Name :
Dosage Form : Lyophilized Powder for Injection
Dosage Strength : 1MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey

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Regulatory Info :
Registration Country : Turkey
Brand Name :
Dosage Form : Lyophilized Powder for Injection
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 2025-12-29
Application Number : 219237
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 2025-12-29
Application Number : 219237
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLOLAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 1995-09-20
Application Number : 20444
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLOLAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 1995-09-20
Application Number : 20444
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : VELETRI
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 2008-06-27
Application Number : 22260
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : VELETRI
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 2012-06-28
Application Number : 22260
Regulatory Info : RX
Registration Country : USA

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Regulatory Info :
Registration Country : Italy
Brand Name : Caripul
Dosage Form : Epoprostenol 0.5Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 0.5 mg + 1 vial solv 100 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info :
Registration Country : Italy
Brand Name : Caripul
Dosage Form : Epoprostenol 1,5Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 1.5 mg + 1 vial solv 100 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 2008-04-23
Application Number : 78396
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 2008-04-23
Application Number : 78396
Regulatory Info : RX
Registration Country : USA

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Regulatory Info :
Registration Country : Italy
Brand Name : Epoprostenol
Dosage Form : Epoprostenol 0.5Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 0.5 mg + 1 vial solv 50 ml + 1 sterile filter
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info :
Registration Country : Italy
Brand Name : Epoprostenol
Dosage Form : Epoprostenol 1,5Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 1.5 mg + 2 vials solv 50 ml + 1 sterile filter
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 2021-01-15
Application Number : 210473
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 2021-01-15
Application Number : 210473
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 0.5MG BASE/VIAL
Packaging :
Approval Date : 2024-06-12
Application Number : 213913
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : EPOPROSTENOL SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1.5MG BASE/VIAL
Packaging :
Approval Date : 2024-06-12
Application Number : 213913
Regulatory Info : RX
Registration Country : USA

Regulatory Info :
Registration Country : Italy
Brand Name : Flolan
Dosage Form : Epoprostenol 1,5Mg 1 Unit Parenteral Use
Dosage Strength : 1 vial EV 1.5 mg + 2 vials solv 50 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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