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1. Cjc 1295
2. Cjc-1295
3. Cjc1295
1. 62rc32v9n7
2. Dtxsid501027567
3. Cjc 1295
| Molecular Weight | 3647.2 g/mol |
|---|---|
| Molecular Formula | C165H269N47O46 |
| XLogP3 | -11.7 |
| Hydrogen Bond Donor Count | 54 |
| Hydrogen Bond Acceptor Count | 52 |
| Rotatable Bond Count | 128 |
| Exact Mass | 3646.0188391 g/mol |
| Monoisotopic Mass | 3645.0154843 g/mol |
| Topological Polar Surface Area | 1540 Ų |
| Heavy Atom Count | 258 |
| Formal Charge | 0 |
| Complexity | 8580 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 33 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A Unii-62RC32V9N7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Unii-62RC32V9N7, including repackagers and relabelers. The FDA regulates Unii-62RC32V9N7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Unii-62RC32V9N7 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 Unii-62RC32V9N7 supplier is an individual or a company that provides Unii-62RC32V9N7 active pharmaceutical ingredient (API) or Unii-62RC32V9N7 finished formulations upon request. The Unii-62RC32V9N7 suppliers may include Unii-62RC32V9N7 API manufacturers, exporters, distributors and traders.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Unii-62RC32V9N7 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Unii-62RC32V9N7 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Unii-62RC32V9N7 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Unii-62RC32V9N7 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Unii-62RC32V9N7 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Unii-62RC32V9N7 suppliers with NDC on PharmaCompass.
Unii-62RC32V9N7 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 Unii-62RC32V9N7 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 Unii-62RC32V9N7 GMP manufacturer or Unii-62RC32V9N7 GMP API supplier for your needs.
A Unii-62RC32V9N7 CoA (Certificate of Analysis) is a formal document that attests to Unii-62RC32V9N7's compliance with Unii-62RC32V9N7 specifications and serves as a tool for batch-level quality control.
Unii-62RC32V9N7 CoA mostly includes findings from lab analyses of a specific batch. For each Unii-62RC32V9N7 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.
Unii-62RC32V9N7 may be tested according to a variety of international standards, such as European Pharmacopoeia (Unii-62RC32V9N7 EP), Unii-62RC32V9N7 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Unii-62RC32V9N7 USP).
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