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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API
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FDF
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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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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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US Patents
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US Exclusivities
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Health Canada Patents
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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
US Medicaid
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| Molecular Weight | 285.26 g/mol |
|---|---|
| Molecular Formula | C10H15N5O5 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 2 |
| Exact Mass | 285.10731860 g/mol |
| Monoisotopic Mass | 285.10731860 g/mol |
| Topological Polar Surface Area | 136 A^2 |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 417 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
API SUPPLIERS
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USDMF
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
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ABOUT THIS PAGE
A 2-Deoxyguanosine Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-Deoxyguanosine Monohydrate, including repackagers and relabelers. The FDA regulates 2-Deoxyguanosine Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-Deoxyguanosine Monohydrate 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 2-Deoxyguanosine Monohydrate supplier is an individual or a company that provides 2-Deoxyguanosine Monohydrate active pharmaceutical ingredient (API) or 2-Deoxyguanosine Monohydrate finished formulations upon request. The 2-Deoxyguanosine Monohydrate suppliers may include 2-Deoxyguanosine Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of 2-Deoxyguanosine Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 2-Deoxyguanosine Monohydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of 2-Deoxyguanosine Monohydrate active pharmaceutical ingredient (API) in detail. Different forms of 2-Deoxyguanosine Monohydrate DMFs exist exist since differing nations have different regulations, such as 2-Deoxyguanosine Monohydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 2-Deoxyguanosine Monohydrate DMF submitted to regulatory agencies in the US is known as a USDMF. 2-Deoxyguanosine Monohydrate USDMF includes data on 2-Deoxyguanosine Monohydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 2-Deoxyguanosine Monohydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 2-Deoxyguanosine Monohydrate suppliers with USDMF on PharmaCompass.
2-Deoxyguanosine Monohydrate 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 2-Deoxyguanosine Monohydrate 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 2-Deoxyguanosine Monohydrate GMP manufacturer or 2-Deoxyguanosine Monohydrate GMP API supplier for your needs.
A 2-Deoxyguanosine Monohydrate CoA (Certificate of Analysis) is a formal document that attests to 2-Deoxyguanosine Monohydrate's compliance with 2-Deoxyguanosine Monohydrate specifications and serves as a tool for batch-level quality control.
2-Deoxyguanosine Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each 2-Deoxyguanosine Monohydrate 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.
2-Deoxyguanosine Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (2-Deoxyguanosine Monohydrate EP), 2-Deoxyguanosine Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2-Deoxyguanosine Monohydrate USP).
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