DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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01 12Dr. Reddy's Laboratories
02 2Actavis Inc
03 4Alembic Pharmaceuticals Limited
04 1Amneal Pharmaceuticals
05 1Amoli Organics
06 1Amomed Pharma Gmbh
07 1Amphastar Pharmaceuticals
08 4Ferrer Internacional
09 4Ferrer International, Sa.
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22 4Scipharm S?rl
23 4Teva Pharmaceutical Industries
24 4Tillomed Laboratories Ltd
25 30United Therapeutics
26 4Zentiva
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01 28INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
02 39Infusion Solution
03 4Infusion fluid, resolution
04 4Injection
05 9POWDER;INHALATION
06 12Perfusion Solution
07 4SOLUTION
08 1SOLUTION;INHALATION
09 4SOLUTION;INTRAVENOUS, SUBCUTANEOUS
10 4Solution For Infusion
11 4Solution For Perfusion
12 2TABLET, EXTENDED RELEASE;ORAL
13 1Treprostinil 100Mg 20Ml 1 Units Parenteral Use
14 1Treprostinil 200Mg 20Ml 1 Units Parenteral Use
15 1Treprostinil 20Mg 20Ml 1 Units Parenteral Use
16 1Treprostinil 50Mg 20Ml 1 Units Parenteral Use
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01 12Allowed
02 20Approved
03 4Authorised
04 16Authorized
05 11DISCN
06 7Deregistered
07 4Lead Market Dossiers- Filed
08 4Prescription
09 31RX
10 10Blank
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01 16REMODULIN
02 23Remodulin
03 22TREPROSTINIL
04 1TYVASO
05 5TYVASO DPI
06 4Treprostinil Ferrer
07 4Treprostinil Ideogen
08 4Treprostinil Orpha
09 4Treprostinil Reddy
10 4Treprostinil Tillomed
11 4Treprostinilo Zentiva
12 8Trepulmix
13 12Tresuvi
14 4YUTREPIA
15 4Blank
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01 4Canada
02 4India
03 4Italy
04 4Malta
05 4Norway
06 16Spain
07 27Sweden
08 12Switzerland
09 44USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : TREPROSTINIL
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2020-05-22
Application Number : 210214
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : TREPROSTINIL
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 2.5MG/ML
Packaging :
Approval Date : 2020-05-22
Application Number : 210214
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : TREPROSTINIL
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 2020-05-22
Application Number : 210214
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : TREPROSTINIL
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 2020-05-22
Application Number : 210214
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 1MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 2.5MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 5MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 10MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Treprostinil Reddy
Dosage Form : Infusion Solution
Dosage Strength : 1mg/ml
Packaging :
Approval Date : 26/01/2022
Application Number : 20200930000055
Regulatory Info : Approved
Registration Country : Sweden
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Treprostinil Reddy
Dosage Form : Infusion Solution
Dosage Strength : 10mg/ml
Packaging :
Approval Date : 26/01/2022
Application Number : 20200930000086
Regulatory Info : Approved
Registration Country : Sweden
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Treprostinil Reddy
Dosage Form : Infusion Solution
Dosage Strength : 2.5mg/ml
Packaging :
Approval Date : 26/01/2022
Application Number : 20200930000062
Regulatory Info : Approved
Registration Country : Sweden
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Treprostinil Reddy
Dosage Form : Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 26/01/2022
Application Number : 20200930000079
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : RX
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2002-05-21
Application Number : 21272
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 2.5MG/ML
Packaging :
Approval Date : 2002-05-21
Application Number : 21272
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 5MG/ML
Packaging :
Approval Date : 2002-05-21
Application Number : 21272
Regulatory Info : RX
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
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Regulatory Info : RX
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 10MG/ML
Packaging :
Approval Date : 2002-05-21
Application Number : 21272
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 20MG/ML
Packaging :
Approval Date : 2021-07-30
Application Number : 21272
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 0.1MG/ML
Packaging :
Approval Date : 2023-09-28
Application Number : 21272
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 0.2MG/ML
Packaging :
Approval Date : 2023-09-28
Application Number : 21272
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
Brand Name : REMODULIN
Dosage Form : INJECTABLE;INTRAVENOUS, SUBCUTANEOUS
Dosage Strength : 0.4MG/ML
Packaging :
Approval Date : 2023-09-28
Application Number : 21272
Regulatory Info : RX
Registration Country : USA
