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| Molecular Weight | 408.6 g/mol |
|---|---|
| Molecular Formula | C24H40O5 |
| XLogP3 | 3.6 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 408.28757437 g/mol |
| Monoisotopic Mass | 408.28757437 g/mol |
| Topological Polar Surface Area | 98 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 637 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 7 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
API SUPPLIERS
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Market Place
ABOUT THIS PAGE
A Ox Bile Extract manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ox Bile Extract, including repackagers and relabelers. The FDA regulates Ox Bile Extract manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ox Bile Extract API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ox Bile Extract manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ox Bile Extract supplier is an individual or a company that provides Ox Bile Extract active pharmaceutical ingredient (API) or Ox Bile Extract finished formulations upon request. The Ox Bile Extract suppliers may include Ox Bile Extract API manufacturers, exporters, distributors and traders.
click here to find a list of Ox Bile Extract suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ox Bile Extract CEP of the European Pharmacopoeia monograph is often referred to as a Ox Bile Extract Certificate of Suitability (COS). The purpose of a Ox Bile Extract CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ox Bile Extract EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ox Bile Extract to their clients by showing that a Ox Bile Extract CEP has been issued for it. The manufacturer submits a Ox Bile Extract CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ox Bile Extract CEP holder for the record. Additionally, the data presented in the Ox Bile Extract CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ox Bile Extract DMF.
A Ox Bile Extract CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ox Bile Extract CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Ox Bile Extract suppliers with CEP (COS) on PharmaCompass.
Ox Bile Extract 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 Ox Bile Extract 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 Ox Bile Extract GMP manufacturer or Ox Bile Extract GMP API supplier for your needs.
A Ox Bile Extract CoA (Certificate of Analysis) is a formal document that attests to Ox Bile Extract's compliance with Ox Bile Extract specifications and serves as a tool for batch-level quality control.
Ox Bile Extract CoA mostly includes findings from lab analyses of a specific batch. For each Ox Bile Extract 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.
Ox Bile Extract may be tested according to a variety of international standards, such as European Pharmacopoeia (Ox Bile Extract EP), Ox Bile Extract JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ox Bile Extract USP).
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