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1. 104169-53-1
2. (8e)-6-ethyl-1,7-dihydroxy-13-methoxy-3,7,9,11-tetramethyl-5,14-dioxabicyclo[11.2.1]hexadec-8-ene-2,4-dione
3. Erythronolide A, 10,11-didehydro-6-demethyl-9-deoxo-3,5,11-trideoxy-6,17-epoxy-4-hydroxy-6-o-methyl-3-oxo-
| Molecular Weight | 398.5 g/mol |
|---|---|
| Molecular Formula | C21H34O7 |
| XLogP3 | 1.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 2 |
| Exact Mass | 398.23045342 g/mol |
| Monoisotopic Mass | 398.23045342 g/mol |
| Topological Polar Surface Area | 102 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 645 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 6 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Neorustmicin B API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Neorustmicin B manufacturer or Neorustmicin B supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Neorustmicin B manufacturer or Neorustmicin B supplier.
A 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE, including repackagers and relabelers. The FDA regulates 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE 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 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE supplier is an individual or a company that provides 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE active pharmaceutical ingredient (API) or 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE finished formulations upon request. The 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE suppliers may include 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE API manufacturers, exporters, distributors and traders.
5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE 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 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE GMP manufacturer or 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE GMP API supplier for your needs.
A 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE CoA (Certificate of Analysis) is a formal document that attests to 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE's compliance with 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE specifications and serves as a tool for batch-level quality control.
5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE CoA mostly includes findings from lab analyses of a specific batch. For each 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE 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.
5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE may be tested according to a variety of international standards, such as European Pharmacopoeia (5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE EP), 5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (5-DESOSAMINYL-6-0-METHYL ERYTHRONOLIDE USP).
