Synopsis
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1. Basic Methacrylate Copolymer
2. Eudragit-e
3. Poly(butylmethacrylate-co-(2-dimethylaminoethyl)methacrylate-co-methyl Methacrylate)
1. 24938-16-7
2. 2-propenoic Acid, 2-methyl-, Butyl Ester, Polymer With 2-(dimethylamino)ethyl 2-methyl-2-propenoate And Methyl 2-methyl-2-propenoate
3. Eudragit E
4. Eudragit-e
5. Butyl 2-methylprop-2-enoate;2-(dimethylamino)ethyl 2-methylprop-2-enoate;methyl 2-methylprop-2-enoate
6. Eudragit E 100
7. Eudragit E 12.5
8. Unii-905hno1sih
9. Amino Methacrylate Copolymer [nf]
10. Eudragit E Po
11. Polyacrylic Resin Iv
12. Basic Methacrylate Copolymer
13. Butyl Methacrylate, Dimethylaminoethyl Methacrylate, Methyl Methacrylate Polymer
14. Butyl Methacrylate, Methyl Methacrylate, Dimethylaminoethyl Methacrylate Polymer
15. 905hno1sih
16. Butyl Methacrylate, Polymer With Methyl Methacrylate And Dimethylaminoethyl Methacrylate
17. Butyl 2-methyl-2-propenoate Polymer With 2-(dimethylamino)ethyl 2-methyl-2-propenoate And Methyl-2-methyl-2-propenoate
18. Schembl427500
19. Poly(butyl Methacrylate-co-dimethylaminoethyl Methacrylate-co-methyl Methacrylate)
20. 2-propenoic Acid, 2-methyl-, Butyl Ester, Polymer With 2-(dimethylamino)ethyl 2-methyl-2-propenoate And Methyl-2-methyl-2-propenoate
21. Methacrylic Acid, Butyl Ester, Polymer With 2-(dimethylamino)ethyl Methacrylate And Methylmethacrylate
22. N,n-dimethylaminoethyl Methacrylate Methyl Methacrylate N-butyl Methacrylate
23. Poly(butylmethacrylate-co-(2-dimethylaminoethyl)methacrylate-co-methyl Methacrylate)
| Molecular Weight | 399.5 g/mol |
|---|---|
| Molecular Formula | C21H37NO6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 12 |
| Exact Mass | 399.26208790 g/mol |
| Monoisotopic Mass | 399.26208790 g/mol |
| Topological Polar Surface Area | 82.1 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 374 |
| 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 | 3 |
API SUPPLIERS
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USDMF
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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ABOUT THIS PAGE
A Eudragit E manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eudragit E, including repackagers and relabelers. The FDA regulates Eudragit E manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eudragit E 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 Eudragit E supplier is an individual or a company that provides Eudragit E active pharmaceutical ingredient (API) or Eudragit E finished formulations upon request. The Eudragit E suppliers may include Eudragit E API manufacturers, exporters, distributors and traders.
click here to find a list of Eudragit E suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Eudragit E DMF (Drug Master File) is a document detailing the whole manufacturing process of Eudragit E active pharmaceutical ingredient (API) in detail. Different forms of Eudragit E DMFs exist exist since differing nations have different regulations, such as Eudragit E USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Eudragit E DMF submitted to regulatory agencies in the US is known as a USDMF. Eudragit E USDMF includes data on Eudragit E's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Eudragit E USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Eudragit E suppliers with USDMF on PharmaCompass.
Eudragit E 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 Eudragit E 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 Eudragit E GMP manufacturer or Eudragit E GMP API supplier for your needs.
A Eudragit E CoA (Certificate of Analysis) is a formal document that attests to Eudragit E's compliance with Eudragit E specifications and serves as a tool for batch-level quality control.
Eudragit E CoA mostly includes findings from lab analyses of a specific batch. For each Eudragit E 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.
Eudragit E may be tested according to a variety of international standards, such as European Pharmacopoeia (Eudragit E EP), Eudragit E JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Eudragit E USP).
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