Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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NDC API
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VMF
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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API
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
1. Djt1116pg
1. 2035989-50-3
2. Olorigliflozin
3. Olorigliflozin [inn]
4. 6fp3nst6zq
5. Chembl5314927
6. Schembl18195012
7. (1r,2s,3s,4r,5s)-5-(4-chloro-3-(4-ethoxybenzyl)phenyl)-1-((r)-1-hydroxyethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol
8. 1,6-anhydro-1-c-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-c-[(1r)-1-hydroxyethyl]-beta-l-idopyranose
9. Beta-l-idopyranose, 1,6-anhydro-1-c-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-c-[(1r)-1-hydroxyethyl]-
| Molecular Weight | 450.9 g/mol |
|---|---|
| Molecular Formula | C23H27ClO7 |
| XLogP3 | 2.1 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 6 |
| Exact Mass | Da |
| Monoisotopic Mass | Da |
| Topological Polar Surface Area | 109 |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 615 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Rongliflozin 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 Rongliflozin manufacturer or Rongliflozin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rongliflozin manufacturer or Rongliflozin supplier.
A Rongliflozin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rongliflozin, including repackagers and relabelers. The FDA regulates Rongliflozin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rongliflozin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Rongliflozin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Rongliflozin supplier is an individual or a company that provides Rongliflozin active pharmaceutical ingredient (API) or Rongliflozin finished formulations upon request. The Rongliflozin suppliers may include Rongliflozin API manufacturers, exporters, distributors and traders.
click here to find a list of Rongliflozin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
Rongliflozin 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 Rongliflozin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Rongliflozin GMP manufacturer or Rongliflozin GMP API supplier for your needs.
A Rongliflozin CoA (Certificate of Analysis) is a formal document that attests to Rongliflozin's compliance with Rongliflozin specifications and serves as a tool for batch-level quality control.
Rongliflozin CoA mostly includes findings from lab analyses of a specific batch. For each Rongliflozin 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.
Rongliflozin may be tested according to a variety of international standards, such as European Pharmacopoeia (Rongliflozin EP), Rongliflozin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rongliflozin USP).
