Synopsis
Synopsis
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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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Listed Suppliers
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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Health Canada Patents
US Medicaid
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz


| Molecular Weight | 149.11 g/mol |
|---|---|
| Molecular Formula | C3H7N3O4 |
| XLogP3 | -3.9 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 3 |
| Exact Mass | 149.04365571 g/mol |
| Monoisotopic Mass | 149.04365571 g/mol |
| Topological Polar Surface Area | 116 A^2 |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 138 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
17
PharmaCompass offers a list of Alanosine 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 Alanosine manufacturer or Alanosine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Alanosine manufacturer or Alanosine supplier.
PharmaCompass also assists you with knowing the Alanosine API Price utilized in the formulation of products. Alanosine API Price is not always fixed or binding as the Alanosine Price is obtained through a variety of data sources. The Alanosine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alanosine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alanosine, including repackagers and relabelers. The FDA regulates Alanosine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alanosine 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 Alanosine supplier is an individual or a company that provides Alanosine active pharmaceutical ingredient (API) or Alanosine finished formulations upon request. The Alanosine suppliers may include Alanosine API manufacturers, exporters, distributors and traders.
click here to find a list of Alanosine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alanosine DMF (Drug Master File) is a document detailing the whole manufacturing process of Alanosine active pharmaceutical ingredient (API) in detail. Different forms of Alanosine DMFs exist exist since differing nations have different regulations, such as Alanosine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Alanosine DMF submitted to regulatory agencies in the US is known as a USDMF. Alanosine USDMF includes data on Alanosine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Alanosine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Alanosine suppliers with USDMF on PharmaCompass.
Alanosine 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 Alanosine 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 Alanosine GMP manufacturer or Alanosine GMP API supplier for your needs.
A Alanosine CoA (Certificate of Analysis) is a formal document that attests to Alanosine's compliance with Alanosine specifications and serves as a tool for batch-level quality control.
Alanosine CoA mostly includes findings from lab analyses of a specific batch. For each Alanosine 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.
Alanosine may be tested according to a variety of international standards, such as European Pharmacopoeia (Alanosine EP), Alanosine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alanosine USP).