Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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Regulatory FDF Prices
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| Molecular Weight | 730.7 g/mol |
|---|---|
| Molecular Formula | C27H46N4O19 |
| XLogP3 | -8.6 |
| Hydrogen Bond Donor Count | 12 |
| Hydrogen Bond Acceptor Count | 20 |
| Rotatable Bond Count | 19 |
| Exact Mass | 730.27562525 g/mol |
| Monoisotopic Mass | 730.27562525 g/mol |
| Topological Polar Surface Area | 365 Ų |
| Heavy Atom Count | 50 |
| Formal Charge | 0 |
| Complexity | 1170 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 13 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |

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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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Regulatory Info :
Registration Country : USA
Brand Name : NEULASTA
Dosage Form : SYRINGE
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 125031
Regulatory Info :
Registration Country : USA

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Regulatory Info : Generic Production in Germany, for Export Markets
Registration Country : Germany
Brand Name :
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 300MCG
Packaging : Vial (Box)
Approval Date :
Application Number : 103353
Regulatory Info : Generic Production in Germany, for Export Markets
Registration Country : Germany

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Regulatory Info : Generic Production in Germany, for Export Markets
Registration Country : Germany
Brand Name :
Dosage Form : SOLUTION FOR INJECTION
Dosage Strength : 480MCG
Packaging : Vial (Box)
Approval Date :
Application Number : 103353
Regulatory Info : Generic Production in Germany, for Export Markets
Registration Country : Germany

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Regulatory Info :
Registration Country : Iran
Brand Name : PegaGen
Dosage Form : Injectable
Dosage Strength : 6MG
Packaging : PFS
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran

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Regulatory Info :
Registration Country : USA
Brand Name : UDENYCA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 761039
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : STIMUFEND
Dosage Form : SOLUTION; INJECTION
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 761173
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : China
Brand Name :
Dosage Form : Injection
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : China

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Regulatory Info :
Registration Country : USA
Brand Name : NYVEPRIA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 761111
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : FYLNETRA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 761084
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : ZIEXTENZO
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 6MG/0.6ML
Packaging :
Approval Date :
Application Number : 761045
Regulatory Info :
Registration Country : USA

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PharmaCompass offers a list of Pegfilgrastim API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pegfilgrastim manufacturer or Pegfilgrastim supplier for your needs.
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A XM22 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of XM22, including repackagers and relabelers. The FDA regulates XM22 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. XM22 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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XM22 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
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