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1. 212pb-dotamtate
2. Dotamtate Pb-212
3. Lead-212 Dotamtate
4. Dotamtate Lead Pb-212
5. E9n7qv53ak
1. 212pb-dotamtate
2. Dotamtate Pb-212
3. Lead-212 Dotamtate
| Molecular Weight | 1642.6 g/mol |
|---|---|
| Molecular Formula | C65H91N17O16PbS2 |
| Hydrogen Bond Donor Count | 15 |
| Hydrogen Bond Acceptor Count | 23 |
| Rotatable Bond Count | 25 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 571 |
| Heavy Atom Count | 101 |
| Formal Charge | 0 |
| Complexity | 2700 |
| Isotope Atom Count | 1 |
| Defined Atom Stereocenter Count | 10 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Alphamedix 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 Alphamedix manufacturer or Alphamedix supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alphamedix manufacturer or Alphamedix supplier.
PharmaCompass also assists you with knowing the Alphamedix API Price utilized in the formulation of products. Alphamedix API Price is not always fixed or binding as the Alphamedix Price is obtained through a variety of data sources. The Alphamedix Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 212pb-dotamtate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 212pb-dotamtate, including repackagers and relabelers. The FDA regulates 212pb-dotamtate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 212pb-dotamtate 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 212pb-dotamtate supplier is an individual or a company that provides 212pb-dotamtate active pharmaceutical ingredient (API) or 212pb-dotamtate finished formulations upon request. The 212pb-dotamtate suppliers may include 212pb-dotamtate API manufacturers, exporters, distributors and traders.
click here to find a list of 212pb-dotamtate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 212pb-dotamtate DMF (Drug Master File) is a document detailing the whole manufacturing process of 212pb-dotamtate active pharmaceutical ingredient (API) in detail. Different forms of 212pb-dotamtate DMFs exist exist since differing nations have different regulations, such as 212pb-dotamtate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 212pb-dotamtate DMF submitted to regulatory agencies in the US is known as a USDMF. 212pb-dotamtate USDMF includes data on 212pb-dotamtate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 212pb-dotamtate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 212pb-dotamtate suppliers with USDMF on PharmaCompass.
212pb-dotamtate 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 212pb-dotamtate 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 212pb-dotamtate GMP manufacturer or 212pb-dotamtate GMP API supplier for your needs.
A 212pb-dotamtate CoA (Certificate of Analysis) is a formal document that attests to 212pb-dotamtate's compliance with 212pb-dotamtate specifications and serves as a tool for batch-level quality control.
212pb-dotamtate CoA mostly includes findings from lab analyses of a specific batch. For each 212pb-dotamtate 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.
212pb-dotamtate may be tested according to a variety of international standards, such as European Pharmacopoeia (212pb-dotamtate EP), 212pb-dotamtate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (212pb-dotamtate USP).
