Synopsis
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NDC API
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1. Ap-23573
2. Ap23573
3. Deforolimus
4. Mk 8669
5. Mk-8669
6. Mk8669
7. Ridaforolimus
1. Deforolimus
| Molecular Weight | 990.2 g/mol |
|---|---|
| Molecular Formula | C53H84NO14P |
| XLogP3 | 5.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 8 |
| Exact Mass | 989.56294335 g/mol |
| Monoisotopic Mass | 989.56294335 g/mol |
| Topological Polar Surface Area | 202 Ų |
| Heavy Atom Count | 69 |
| Formal Charge | 0 |
| Complexity | 1940 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 15 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Ridaforolimus 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 Ridaforolimus manufacturer or Ridaforolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ridaforolimus manufacturer or Ridaforolimus supplier.
PharmaCompass also assists you with knowing the Ridaforolimus API Price utilized in the formulation of products. Ridaforolimus API Price is not always fixed or binding as the Ridaforolimus Price is obtained through a variety of data sources. The Ridaforolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MK8669 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK8669, including repackagers and relabelers. The FDA regulates MK8669 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK8669 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 MK8669 supplier is an individual or a company that provides MK8669 active pharmaceutical ingredient (API) or MK8669 finished formulations upon request. The MK8669 suppliers may include MK8669 API manufacturers, exporters, distributors and traders.
click here to find a list of MK8669 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MK8669 DMF (Drug Master File) is a document detailing the whole manufacturing process of MK8669 active pharmaceutical ingredient (API) in detail. Different forms of MK8669 DMFs exist exist since differing nations have different regulations, such as MK8669 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MK8669 DMF submitted to regulatory agencies in the US is known as a USDMF. MK8669 USDMF includes data on MK8669's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MK8669 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MK8669 suppliers with USDMF on PharmaCompass.
MK8669 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 MK8669 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 MK8669 GMP manufacturer or MK8669 GMP API supplier for your needs.
A MK8669 CoA (Certificate of Analysis) is a formal document that attests to MK8669's compliance with MK8669 specifications and serves as a tool for batch-level quality control.
MK8669 CoA mostly includes findings from lab analyses of a specific batch. For each MK8669 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.
MK8669 may be tested according to a variety of international standards, such as European Pharmacopoeia (MK8669 EP), MK8669 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MK8669 USP).
