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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
A Pevikon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pevikon, including repackagers and relabelers. The FDA regulates Pevikon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pevikon 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 Pevikon supplier is an individual or a company that provides Pevikon active pharmaceutical ingredient (API) or Pevikon finished formulations upon request. The Pevikon suppliers may include Pevikon API manufacturers, exporters, distributors and traders.
click here to find a list of Pevikon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pevikon DMF (Drug Master File) is a document detailing the whole manufacturing process of Pevikon active pharmaceutical ingredient (API) in detail. Different forms of Pevikon DMFs exist exist since differing nations have different regulations, such as Pevikon USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pevikon DMF submitted to regulatory agencies in the US is known as a USDMF. Pevikon USDMF includes data on Pevikon's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pevikon USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Pevikon suppliers with USDMF on PharmaCompass.
Pevikon 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 Pevikon 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 Pevikon GMP manufacturer or Pevikon GMP API supplier for your needs.
A Pevikon CoA (Certificate of Analysis) is a formal document that attests to Pevikon's compliance with Pevikon specifications and serves as a tool for batch-level quality control.
Pevikon CoA mostly includes findings from lab analyses of a specific batch. For each Pevikon 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.
Pevikon may be tested according to a variety of international standards, such as European Pharmacopoeia (Pevikon EP), Pevikon JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pevikon USP).
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