Aspen API. More than just an API™

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01 5Aspen API
02 7Aspen Pharmacare Holdings
03 4Dr. Reddy's Laboratories
04 4Aurobindo Pharma Limited
05 1BrightGene Bio-Medical Technology Co.,Ltd
06 1Farmak JSC
07 5GSK
08 4Hangzhou Zhongmei Huadong Pharmaceutical
09 8Jiangsu Hengrui Medicine
10 1Lotus Pharmaceutical Industries
11 4ScinoPharm Taiwan Ltd
12 40Viatris
13 4XYZ Pharma
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01 1Fondaparinux 1,5Mg 0,3Ml 10 Units Parenteral Use
02 1Fondaparinux 10Mg 0,8Ml 10 Units Parenteral Use
03 1Fondaparinux 2,5Mg 0,5Ml 10 Inita' Parenteral Use
04 1Fondaparinux 5Mg 0.4 Ml 10 Units Parenteral Use
05 1Fondaparinux 7,5Mg 0,6Ml 10 Units Parenteral Use
06 4INJ
07 25INJECTABLE;SUBCUTANEOUS
08 4Injectable
09 5Injectable Solution In Pre-Filled Syringe
10 3Injectable Solution in Pre-Filled Syringe
11 5Injection
12 1Prefilled Syringe
13 2SOLUTION
14 33Solution For Injection
15 1Blank
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01 5Allowed
02 5Approved
03 8Authorized
04 5DISCN
05 5Deregistered
06 2Generic
07 1Marketed
08 5Not Marketed
09 3Originator
10 12Prescription
11 20RX
12 4US FDA Preapproval Inspection- Pass
13 13Blank
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01 6ARIXTRA
02 35Arixtra
03 5Arixtra
04 1Arixtra 10,0mg/0,8ml
05 1Arixtra 2,5 mg/0,5 ml
06 1Arixtra 5,0mg/0,4ml
07 1Arixtra 7,5mg/0,6ml
08 2Arixtra®
09 21FONDAPARINUX SODIUM
10 4Fondaparinux
11 1Product Under Development
12 5Quixidar
13 5Blank
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01 1Australia
02 2Canada
03 4China
04 5Denmark
05 1Egypt
06 5Estonia
07 4India
08 5Italy
09 2Moldova
10 6Norway
11 4South Africa
12 8Spain
13 10Sweden
14 5Switzerland
15 25USA
16 1Ukraine
Regulatory Info :
Registration Country : Italy
Brand Name : Arixtra
Dosage Form : Fondaparinux 1,5Mg 0,3Ml 10 Units Parenteral Use
Dosage Strength : 10 SYRINGES SC 1.5 mg 0.3 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : ARIXTRA
Dosage Form : SOLUTION
Dosage Strength : 2.5MG/0.5ML
Packaging : 0.5ML
Approval Date :
Application Number : 2245531
Regulatory Info : Prescription
Registration Country : Canada
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : India
Brand Name : Fondaparinux
Dosage Form : Injectable
Dosage Strength : 2.5 mg / 0.5 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : Italy
Brand Name : Arixtra
Dosage Form : Fondaparinux 10Mg 0,8Ml 10 Units Parenteral Use
Dosage Strength : 10 SYRINGES SC 10 mg 0.8 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Arixtra
Dosage Form : Fondaparinux 2,5Mg 0,5Ml 10 Inita' Parenteral Use
Dosage Strength : 10 SYRINGES SC 2.5 mg 0.5 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Arixtra
Dosage Form : Fondaparinux 5Mg 0.4 Ml 10 Units Parenteral Use
Dosage Strength : 10 SYRINGES SC 5 mg 0.4 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Arixtra
Dosage Form : Fondaparinux 7,5Mg 0,6Ml 10 Units Parenteral Use
Dosage Strength : 10 SYRINGES SC 7.5 mg 0.6 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : ARIXTRA
Dosage Form : SOLUTION
Dosage Strength : 7.5MG/0.6ML
Packaging : 0.6ML
Approval Date :
Application Number : 2258056
Regulatory Info : Prescription
Registration Country : Canada
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Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Arixtra 2,5 mg/0,5 ml
Dosage Form : INJ
Dosage Strength : 2.5mg/0.5ml
Packaging : 0.5X10mg/0.5ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Arixtra 5,0mg/0,4ml
Dosage Form : INJ
Dosage Strength : 5mg/0.4ml
Packaging : 0.4X10mg/0.4ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Arixtra 7,5mg/0,6ml
Dosage Form : INJ
Dosage Strength : 7.5mg/0.6ml
Packaging : 0.6X10mg/0.6ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
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Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Arixtra 10,0mg/0,8ml
Dosage Form : INJ
Dosage Strength : 10mg/0.8ml
Packaging : 0.8X10mg/0.8ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
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Regulatory Info :
Registration Country : Australia
Brand Name : Arixtra
Dosage Form :
Dosage Strength :
Packaging : 2
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : India
Brand Name : Fondaparinux
Dosage Form : Injectable
Dosage Strength : 5 mg / 0.4 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : India
Brand Name : Fondaparinux
Dosage Form : Injectable
Dosage Strength : 7.5 mg / 0.6 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : India
Brand Name : Fondaparinux
Dosage Form : Injectable
Dosage Strength : 10 mg / 0.8 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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Regulatory Info : RX
Registration Country : USA
Brand Name : ARIXTRA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 2.5MG/0.5ML
Packaging :
Approval Date : 2001-12-07
Application Number : 21345
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : ARIXTRA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 5MG/0.4ML
Packaging :
Approval Date : 2004-05-28
Application Number : 21345
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : ARIXTRA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 7.5MG/0.6ML
Packaging :
Approval Date : 2004-05-28
Application Number : 21345
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : ARIXTRA
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 10MG/0.8ML
Packaging :
Approval Date : 2004-05-28
Application Number : 21345
Regulatory Info : RX
Registration Country : USA
