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1. Z9slp4ow0y
2. 1438895-00-1
3. L-glutamic Acid, N-(4-(2-(2-amino-4,7-dihydro-4-oxo-3h-pyrrolo(2,3-d)pyrimidin-5-yl)ethyl)benzoyl)-, Potassium Salt (1:2)
4. Unii-z9slp4ow0y
5. Schembl15649196
| Molecular Weight | 503.6 g/mol |
|---|---|
| Molecular Formula | C20H19K2N5O6 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 7 |
| Exact Mass | 503.0609463 g/mol |
| Monoisotopic Mass | 503.0609463 g/mol |
| Topological Polar Surface Area | 193 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 737 |
| 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 | 3 |
API SUPPLIERS
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ABOUT THIS PAGE
A Pemetrexed Dipotassium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pemetrexed Dipotassium, including repackagers and relabelers. The FDA regulates Pemetrexed Dipotassium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pemetrexed Dipotassium 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 Dipotassium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pemetrexed Dipotassium supplier is an individual or a company that provides Pemetrexed Dipotassium active pharmaceutical ingredient (API) or Pemetrexed Dipotassium finished formulations upon request. The Pemetrexed Dipotassium suppliers may include Pemetrexed Dipotassium API manufacturers, exporters, distributors and traders.
click here to find a list of Pemetrexed Dipotassium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pemetrexed Dipotassium DMF (Drug Master File) is a document detailing the whole manufacturing process of Pemetrexed Dipotassium active pharmaceutical ingredient (API) in detail. Different forms of Pemetrexed Dipotassium DMFs exist exist since differing nations have different regulations, such as Pemetrexed Dipotassium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pemetrexed Dipotassium DMF submitted to regulatory agencies in the US is known as a USDMF. Pemetrexed Dipotassium USDMF includes data on Pemetrexed Dipotassium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pemetrexed Dipotassium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pemetrexed Dipotassium suppliers with USDMF on PharmaCompass.
Pemetrexed Dipotassium 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 Dipotassium 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 Dipotassium GMP manufacturer or Pemetrexed Dipotassium GMP API supplier for your needs.
A Pemetrexed Dipotassium CoA (Certificate of Analysis) is a formal document that attests to Pemetrexed Dipotassium's compliance with Pemetrexed Dipotassium specifications and serves as a tool for batch-level quality control.
Pemetrexed Dipotassium CoA mostly includes findings from lab analyses of a specific batch. For each Pemetrexed Dipotassium 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 Dipotassium may be tested according to a variety of international standards, such as European Pharmacopoeia (Pemetrexed Dipotassium EP), Pemetrexed Dipotassium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pemetrexed Dipotassium USP).
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