Synopsis
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| Molecular Weight | 772.8 g/mol |
|---|---|
| Molecular Formula | C42H46F2N4O8 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 16 |
| Exact Mass | 772.32837076 g/mol |
| Monoisotopic Mass | 772.32837076 g/mol |
| Topological Polar Surface Area | 158 A^2 |
| Heavy Atom Count | 56 |
| Formal Charge | 0 |
| Complexity | 651 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 3 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
ABOUT THIS PAGE
A Eplivanserin Hemifumarate Salt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eplivanserin Hemifumarate Salt, including repackagers and relabelers. The FDA regulates Eplivanserin Hemifumarate Salt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eplivanserin Hemifumarate Salt 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 Eplivanserin Hemifumarate Salt supplier is an individual or a company that provides Eplivanserin Hemifumarate Salt active pharmaceutical ingredient (API) or Eplivanserin Hemifumarate Salt finished formulations upon request. The Eplivanserin Hemifumarate Salt suppliers may include Eplivanserin Hemifumarate Salt API manufacturers, exporters, distributors and traders.
click here to find a list of Eplivanserin Hemifumarate Salt suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eplivanserin Hemifumarate Salt DMF (Drug Master File) is a document detailing the whole manufacturing process of Eplivanserin Hemifumarate Salt active pharmaceutical ingredient (API) in detail. Different forms of Eplivanserin Hemifumarate Salt DMFs exist exist since differing nations have different regulations, such as Eplivanserin Hemifumarate Salt USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eplivanserin Hemifumarate Salt DMF submitted to regulatory agencies in the US is known as a USDMF. Eplivanserin Hemifumarate Salt USDMF includes data on Eplivanserin Hemifumarate Salt's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eplivanserin Hemifumarate Salt USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eplivanserin Hemifumarate Salt suppliers with USDMF on PharmaCompass.
Eplivanserin Hemifumarate Salt 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 Eplivanserin Hemifumarate Salt 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 Eplivanserin Hemifumarate Salt GMP manufacturer or Eplivanserin Hemifumarate Salt GMP API supplier for your needs.
A Eplivanserin Hemifumarate Salt CoA (Certificate of Analysis) is a formal document that attests to Eplivanserin Hemifumarate Salt's compliance with Eplivanserin Hemifumarate Salt specifications and serves as a tool for batch-level quality control.
Eplivanserin Hemifumarate Salt CoA mostly includes findings from lab analyses of a specific batch. For each Eplivanserin Hemifumarate Salt 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.
Eplivanserin Hemifumarate Salt may be tested according to a variety of international standards, such as European Pharmacopoeia (Eplivanserin Hemifumarate Salt EP), Eplivanserin Hemifumarate Salt JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eplivanserin Hemifumarate Salt USP).
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