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1. Sel24-b489
2. Sel-24 Free Base
3. 9m7x64vtli
4. Sel24-b289
5. 1616359-00-2
6. 1h-benzimidazole, 5,6-dibromo-1-(1-methylethyl)-4-nitro-2-(4-piperidinyl)-
7. 5,6-dibromo-1-(1-methylethyl)-4-nitro-2-(4-piperidinyl)-1h-benzimidazole
8. 5,6-dibromo-4-nitro-2-(piperidin-4-yl)-1-(propan-2-yl)-1h-1,3-benzimidazole
9. Unii-9m7x64vtli
10. Chembl4467168
11. Schembl15826208
12. Hy-120758
13. Cs-0079085
| Molecular Weight | 446.14 g/mol |
|---|---|
| Molecular Formula | C15H18Br2N4O2 |
| XLogP3 | 3.5 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 445.97760 g/mol |
| Monoisotopic Mass | 443.97965 g/mol |
| Topological Polar Surface Area | 75.7 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 442 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A MEN1703 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MEN1703, including repackagers and relabelers. The FDA regulates MEN1703 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MEN1703 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 MEN1703 supplier is an individual or a company that provides MEN1703 active pharmaceutical ingredient (API) or MEN1703 finished formulations upon request. The MEN1703 suppliers may include MEN1703 API manufacturers, exporters, distributors and traders.
MEN1703 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 MEN1703 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 MEN1703 GMP manufacturer or MEN1703 GMP API supplier for your needs.
A MEN1703 CoA (Certificate of Analysis) is a formal document that attests to MEN1703's compliance with MEN1703 specifications and serves as a tool for batch-level quality control.
MEN1703 CoA mostly includes findings from lab analyses of a specific batch. For each MEN1703 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.
MEN1703 may be tested according to a variety of international standards, such as European Pharmacopoeia (MEN1703 EP), MEN1703 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MEN1703 USP).
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