Synopsis
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| Molecular Weight | 5685 g/mol |
|---|---|
| Molecular Formula | C172H221N62O91P17S17 |
| XLogP3 | -9 |
| Hydrogen Bond Donor Count | 41 |
| Hydrogen Bond Acceptor Count | 124 |
| Rotatable Bond Count | 104 |
| Exact Mass | 5681.5396694 g/mol |
| Monoisotopic Mass | 5680.5363146 g/mol |
| Topological Polar Surface Area | 2520 A^2 |
| Heavy Atom Count | 359 |
| Formal Charge | 0 |
| Complexity | 16500 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 54 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Oblimersen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oblimersen, including repackagers and relabelers. The FDA regulates Oblimersen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oblimersen API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Oblimersen supplier is an individual or a company that provides Oblimersen active pharmaceutical ingredient (API) or Oblimersen finished formulations upon request. The Oblimersen suppliers may include Oblimersen API manufacturers, exporters, distributors and traders.
click here to find a list of Oblimersen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oblimersen DMF (Drug Master File) is a document detailing the whole manufacturing process of Oblimersen active pharmaceutical ingredient (API) in detail. Different forms of Oblimersen DMFs exist exist since differing nations have different regulations, such as Oblimersen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oblimersen DMF submitted to regulatory agencies in the US is known as a USDMF. Oblimersen USDMF includes data on Oblimersen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oblimersen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oblimersen suppliers with USDMF on PharmaCompass.
Oblimersen 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).
PharmaCompass offers a list of Oblimersen GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Oblimersen GMP manufacturer or Oblimersen GMP API supplier for your needs.
A Oblimersen CoA (Certificate of Analysis) is a formal document that attests to Oblimersen's compliance with Oblimersen specifications and serves as a tool for batch-level quality control.
Oblimersen CoA mostly includes findings from lab analyses of a specific batch. For each Oblimersen CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Oblimersen may be tested according to a variety of international standards, such as European Pharmacopoeia (Oblimersen EP), Oblimersen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Oblimersen USP).
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