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1. Arm210
2. Arm-210
3. S48168
4. S-48168
5. 1033gn605l
6. 4-((7-methoxy-2,3-dihydro-1,4-benzothiazepin-4(5h)-yl)methyl)benzoic Acid
7. 4-[(7-methoxy-2,3-dihydro-1,4-benzothiazepin-4(5h)-yl)methyl]benzoic Acid
8. Benzoic Acid, 4-((2,3-dihydro-7-methoxy-1,4-benzothiazepin-4(5h)-yl)methyl)-
9. 1467605-57-7
10. Chembl4594418
11. Schembl15326996
12. Unii-1033gn605l
13. 4-((7-methoxy-2,3-dihydrobenzo[f][1,4]thiazepin-4(5h)-yl)methyl)benzoic Acid
| Molecular Weight | 329.4 g/mol |
|---|---|
| Molecular Formula | C18H19NO3S |
| XLogP3 | 0.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 329.10856464 g/mol |
| Monoisotopic Mass | 329.10856464 g/mol |
| Topological Polar Surface Area | 75.1 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 398 |
| 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 ARM210 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ARM210, including repackagers and relabelers. The FDA regulates ARM210 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ARM210 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 ARM210 supplier is an individual or a company that provides ARM210 active pharmaceutical ingredient (API) or ARM210 finished formulations upon request. The ARM210 suppliers may include ARM210 API manufacturers, exporters, distributors and traders.
ARM210 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 ARM210 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 ARM210 GMP manufacturer or ARM210 GMP API supplier for your needs.
A ARM210 CoA (Certificate of Analysis) is a formal document that attests to ARM210's compliance with ARM210 specifications and serves as a tool for batch-level quality control.
ARM210 CoA mostly includes findings from lab analyses of a specific batch. For each ARM210 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.
ARM210 may be tested according to a variety of international standards, such as European Pharmacopoeia (ARM210 EP), ARM210 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ARM210 USP).
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