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1. Pemetrexed Tromethamine
2. Uw86gb537a
3. Pemetrexed Tromethamine [usan]
4. 1851348-04-3
5. Pemetrexed Tromethamine (usan)
6. L-glutamic Acid, N-(4-(2-(2-amino-4,7-dihydro-4-oxo-3h-pyrrolo(2,3-d)pyrimidin-5-yl)ethyl)benzoyl)-, Compd. With 2-amino-2-(hydroxymethyl)-1,3-propanediol, Hydrate (1:2:2)
7. Unii-uw86gb537a
8. Chembl3989962
9. D11352
10. Pemetrexed Ditromethamine Dihydrate [who-dd]
11. Q27291301
12. N-(4-(2-(2-amino-4-oxo-4,7-dihydro-1h-pyrrolo(2,3-d)pyrimidin-5-yl)ethyl)benzoyl)-l-glutamic Acid Bis(2-amino-2-(hydroxymethyl)propane-1,3-diol) Salt, Dihydrate
Molecular Weight | 705.7 g/mol |
---|---|
Molecular Formula | C28H47N7O14 |
Hydrogen Bond Donor Count | 16 |
Hydrogen Bond Acceptor Count | 17 |
Rotatable Bond Count | 15 |
Exact Mass | 705.31809920 g/mol |
Monoisotopic Mass | 705.31809920 g/mol |
Topological Polar Surface Area | 362 Ų |
Heavy Atom Count | 49 |
Formal Charge | 0 |
Complexity | 802 |
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 | 5 |
Market Place
ABOUT THIS PAGE
A Pemetrexed Ditromethamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pemetrexed Ditromethamine, including repackagers and relabelers. The FDA regulates Pemetrexed Ditromethamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pemetrexed Ditromethamine 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 Pemetrexed Ditromethamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pemetrexed Ditromethamine supplier is an individual or a company that provides Pemetrexed Ditromethamine active pharmaceutical ingredient (API) or Pemetrexed Ditromethamine finished formulations upon request. The Pemetrexed Ditromethamine suppliers may include Pemetrexed Ditromethamine API manufacturers, exporters, distributors and traders.
click here to find a list of Pemetrexed Ditromethamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pemetrexed Ditromethamine written confirmation (Pemetrexed Ditromethamine WC) is an official document issued by a regulatory agency to a Pemetrexed Ditromethamine manufacturer, verifying that the manufacturing facility of a Pemetrexed Ditromethamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pemetrexed Ditromethamine APIs or Pemetrexed Ditromethamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Pemetrexed Ditromethamine WC (written confirmation) as part of the regulatory process.
click here to find a list of Pemetrexed Ditromethamine suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Pemetrexed Ditromethamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pemetrexed Ditromethamine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Pemetrexed Ditromethamine as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Pemetrexed Ditromethamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pemetrexed Ditromethamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pemetrexed Ditromethamine suppliers with NDC on PharmaCompass.
Pemetrexed Ditromethamine 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 Pemetrexed Ditromethamine 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 Pemetrexed Ditromethamine GMP manufacturer or Pemetrexed Ditromethamine GMP API supplier for your needs.
A Pemetrexed Ditromethamine CoA (Certificate of Analysis) is a formal document that attests to Pemetrexed Ditromethamine's compliance with Pemetrexed Ditromethamine specifications and serves as a tool for batch-level quality control.
Pemetrexed Ditromethamine CoA mostly includes findings from lab analyses of a specific batch. For each Pemetrexed Ditromethamine 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.
Pemetrexed Ditromethamine may be tested according to a variety of international standards, such as European Pharmacopoeia (Pemetrexed Ditromethamine EP), Pemetrexed Ditromethamine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pemetrexed Ditromethamine USP).
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