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1. 181924b87f
2. Q27251958
3. Closantel Sodium Dihydrate For Veterinary Use [ep Impurity]
4. Closantel Sodium Dihydrate For Veterinary Use [ep Monograph]
5. 5'-chloro-4'-(4-chloro-.alpha.-cyanobenzyl)-3,5-di-iodosalicyl-o-toluidide Sodium Dihydrate
| Molecular Weight | 721.1 g/mol |
|---|---|
| Molecular Formula | C22H17Cl2I2N2NaO4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 719.85525 g/mol |
| Monoisotopic Mass | 719.85525 g/mol |
| Topological Polar Surface Area | 78 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 659 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 4 |
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ABOUT THIS PAGE
A 2331Ah manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2331Ah, including repackagers and relabelers. The FDA regulates 2331Ah manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2331Ah 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 2331Ah supplier is an individual or a company that provides 2331Ah active pharmaceutical ingredient (API) or 2331Ah finished formulations upon request. The 2331Ah suppliers may include 2331Ah API manufacturers, exporters, distributors and traders.
2331Ah 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 2331Ah 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 2331Ah GMP manufacturer or 2331Ah GMP API supplier for your needs.
A 2331Ah CoA (Certificate of Analysis) is a formal document that attests to 2331Ah's compliance with 2331Ah specifications and serves as a tool for batch-level quality control.
2331Ah CoA mostly includes findings from lab analyses of a specific batch. For each 2331Ah 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.
2331Ah may be tested according to a variety of international standards, such as European Pharmacopoeia (2331Ah EP), 2331Ah JP (Japanese Pharmacopeia) and the US Pharmacopoeia (2331Ah USP).
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