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1. Erythrityl Tetranitrate
2. Tetranitrate, Erythrityl
1. Erythrityl Tetranitrate
2. Cardiloid
3. Cardivell
4. Cardiwell
5. Erythritetranitrat
6. 1,3,4-trinitrooxybutan-2-yl Nitrate
7. Erythritol, Tetranitrate
8. 7297-25-8
9. Schembl613474
10. Chembl453636
11. 1,2,3,4-butanetetrayl Nitrate
12. Dtxsid20860007
13. 1,3,4-butanetetralyl Tetranitrate
14. Nsc106566
15. Butane-1,2,3,4-tetrayl Tetranitrate
16. 643-97-0
17. 1,3,4-butanetetrol, Tetranitrate, (r*,s*)-
| Molecular Weight | 302.11 g/mol |
|---|---|
| Molecular Formula | C4H6N4O12 |
| XLogP3 | 1.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 7 |
| Exact Mass | 301.99822164 g/mol |
| Monoisotopic Mass | 301.99822164 g/mol |
| Topological Polar Surface Area | 220 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 326 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Vasodilator Agents
Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)
ABOUT THIS PAGE
A Erythrityl Tetranitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erythrityl Tetranitrate, including repackagers and relabelers. The FDA regulates Erythrityl Tetranitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erythrityl Tetranitrate 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 Erythrityl Tetranitrate supplier is an individual or a company that provides Erythrityl Tetranitrate active pharmaceutical ingredient (API) or Erythrityl Tetranitrate finished formulations upon request. The Erythrityl Tetranitrate suppliers may include Erythrityl Tetranitrate API manufacturers, exporters, distributors and traders.
click here to find a list of Erythrityl Tetranitrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Erythrityl Tetranitrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Erythrityl Tetranitrate active pharmaceutical ingredient (API) in detail. Different forms of Erythrityl Tetranitrate DMFs exist exist since differing nations have different regulations, such as Erythrityl Tetranitrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Erythrityl Tetranitrate DMF submitted to regulatory agencies in the US is known as a USDMF. Erythrityl Tetranitrate USDMF includes data on Erythrityl Tetranitrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Erythrityl Tetranitrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Erythrityl Tetranitrate suppliers with USDMF on PharmaCompass.
Erythrityl Tetranitrate 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 Erythrityl Tetranitrate 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 Erythrityl Tetranitrate GMP manufacturer or Erythrityl Tetranitrate GMP API supplier for your needs.
A Erythrityl Tetranitrate CoA (Certificate of Analysis) is a formal document that attests to Erythrityl Tetranitrate's compliance with Erythrityl Tetranitrate specifications and serves as a tool for batch-level quality control.
Erythrityl Tetranitrate CoA mostly includes findings from lab analyses of a specific batch. For each Erythrityl Tetranitrate 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.
Erythrityl Tetranitrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Erythrityl Tetranitrate EP), Erythrityl Tetranitrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Erythrityl Tetranitrate USP).
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