Synopsis
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1. Poly(vinyl Chloride)-poly(vinyl Acetate) Copolymer
2. Polyvinylchloride-polyvinylacetate Copolymer
3. Pvc-pvac
4. Rhodopas Ax
1. Vinyl Chloride-vinyl Acetate Copolymer
2. 9003-22-9
3. Chloroethene;ethenyl Acetate
4. Tygon
5. Vinyl Chloride/vinyl Acetate Copolymer
6. Vinyl Chloride-vinyl Acetate
7. Vinyl Chloride Vinyl Acetate Polymer
8. Vinyl Acetate Vinyl Chloride
9. Vinyl Chloride Vinyl Acetate
10. Schembl27942
11. Chebi:82549
12. Akos024319180
13. Poly(limonene-co-beta-pinene), Hydrogenated
14. C19546
15. Vinylidene Chloride-2-ethylhexyl Acrylate Copolymer
16. 106168-37-0
17. 28431-58-5
| Molecular Weight | 148.59 g/mol |
|---|---|
| Molecular Formula | C6H9ClO2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 148.0291072 g/mol |
| Monoisotopic Mass | 148.0291072 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 76.2 |
| 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 | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Pevikon 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 Pevikon manufacturer or Pevikon supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pevikon manufacturer or Pevikon supplier.
A Solvic PA 513 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solvic PA 513, including repackagers and relabelers. The FDA regulates Solvic PA 513 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solvic PA 513 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 Solvic PA 513 supplier is an individual or a company that provides Solvic PA 513 active pharmaceutical ingredient (API) or Solvic PA 513 finished formulations upon request. The Solvic PA 513 suppliers may include Solvic PA 513 API manufacturers, exporters, distributors and traders.
click here to find a list of Solvic PA 513 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Solvic PA 513 DMF (Drug Master File) is a document detailing the whole manufacturing process of Solvic PA 513 active pharmaceutical ingredient (API) in detail. Different forms of Solvic PA 513 DMFs exist exist since differing nations have different regulations, such as Solvic PA 513 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Solvic PA 513 DMF submitted to regulatory agencies in the US is known as a USDMF. Solvic PA 513 USDMF includes data on Solvic PA 513's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Solvic PA 513 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Solvic PA 513 suppliers with USDMF on PharmaCompass.
Solvic PA 513 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 Solvic PA 513 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Solvic PA 513 GMP manufacturer or Solvic PA 513 GMP API supplier for your needs.
A Solvic PA 513 CoA (Certificate of Analysis) is a formal document that attests to Solvic PA 513's compliance with Solvic PA 513 specifications and serves as a tool for batch-level quality control.
Solvic PA 513 CoA mostly includes findings from lab analyses of a specific batch. For each Solvic PA 513 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.
Solvic PA 513 may be tested according to a variety of international standards, such as European Pharmacopoeia (Solvic PA 513 EP), Solvic PA 513 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Solvic PA 513 USP).
