Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. 5897-66-5
2. C229n9dx94
3. 1,3-dimethyl-7h-purine-2,6-dione;ethane-1,2-diamine;dihydrate
4. 1,3-dimethyl-3,7-dihydro-1h-purine-2,6-dione Hemiethane-1,2-diamine Salt Dihydrate
5. Amirophylline
6. Unii-c229n9dx94
7. 72487-55-9
8. Niosh/xh5602000
9. Dtxsid50207709
10. Theophylline-ethylenediamine Hydrate
11. Aminophylline Dihydrate [vandf]
12. Aminophylline Dihydrate [who-dd]
13. Xh56020000
14. Aminophylline Dihydrate [usp Monograph]
15. D11630
16. Theophylline And Ethylenediamine Hydrate
17. Q27275080
18. Theophylline, Compd. With Ethylenediamine, Hydrate (2:1:2)
19. Theophylline-ethylenediamine Dihydrate [ep Monograph]
20. 1,3-dimethyl-1h-purine-2,6(3h,9h)-dione Compound With Ethane-1,2-diamine (2:1) Dihydrate
| Molecular Weight | 456.46 g/mol |
|---|---|
| Molecular Formula | C16H28N10O6 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 1 |
| Exact Mass | 456.21932865 g/mol |
| Monoisotopic Mass | 456.21932865 g/mol |
| Topological Polar Surface Area | 193 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 273 |
| 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 | 5 |
ABOUT THIS PAGE
A Amirophylline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amirophylline, including repackagers and relabelers. The FDA regulates Amirophylline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amirophylline 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 Amirophylline supplier is an individual or a company that provides Amirophylline active pharmaceutical ingredient (API) or Amirophylline finished formulations upon request. The Amirophylline suppliers may include Amirophylline API manufacturers, exporters, distributors and traders.
Amirophylline 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 Amirophylline 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 Amirophylline GMP manufacturer or Amirophylline GMP API supplier for your needs.
A Amirophylline CoA (Certificate of Analysis) is a formal document that attests to Amirophylline's compliance with Amirophylline specifications and serves as a tool for batch-level quality control.
Amirophylline CoA mostly includes findings from lab analyses of a specific batch. For each Amirophylline 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.
Amirophylline may be tested according to a variety of international standards, such as European Pharmacopoeia (Amirophylline EP), Amirophylline JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Amirophylline USP).
LOOKING FOR A SUPPLIER?
