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

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01 1NanoAlvand
02 12care4
03 2Campus Pharma AB
04 2Centocor
05 2Central Procurement & Supplies Unit
06 2Ebb Medical
07 2Farmatek
08 2GLAND PHARMA LIMITED
09 9GSK
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11 8Johnson & Johnson Innovative Medicine
12 2LABORATORIOS NORMON SA
13 2Meitheal Pharmaceuticals
14 2NTC
15 4Sun Pharmaceutical Industries Limited
16 2Viatris
17 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 6Solution For Injection
11 5Blank
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01 2Allowed
02 2Authorised
03 5Authorized
04 2Cancelled
05 2DISCN
06 4Deregistered
07 8Prescription
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 8Flolan
12 2VELETRI
13 11Veletri
14 2Blank
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01 4Australia
02 4Canada
03 3Denmark
04 1Estonia
05 1Iran
06 5Italy
07 3Malta
08 9Spain
09 4Sweden
10 2Switzerland
11 2Turkey
12 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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