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1. Ombitasvir & Paritaprevir & Ritonavir
2. Ombitasvir + Paritaprevir + Ritonavir
3. Ombitasvir / Paritaprevir / Ritonavir
4. Ombitasvir And Paritaprevir And Ritonavir
5. Ombitasvir Mixture With Paritaprevir And Ritonavir
6. S900007110
| Molecular Weight | 2380.9 g/mol |
|---|---|
| Molecular Formula | C127H158N20O20S3 |
| Hydrogen Bond Donor Count | 11 |
| Hydrogen Bond Acceptor Count | 28 |
| Rotatable Bond Count | 41 |
| Exact Mass | 2380.11569587 g/mol |
| Monoisotopic Mass | 2379.11234103 g/mol |
| Topological Polar Surface Area | 579 Ų |
| Heavy Atom Count | 170 |
| Formal Charge | 0 |
| Complexity | 4190 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 13 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
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ABOUT THIS PAGE
A Technivie manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Technivie, including repackagers and relabelers. The FDA regulates Technivie manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Technivie 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 Technivie supplier is an individual or a company that provides Technivie active pharmaceutical ingredient (API) or Technivie finished formulations upon request. The Technivie suppliers may include Technivie API manufacturers, exporters, distributors and traders.
Technivie 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 Technivie 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 Technivie GMP manufacturer or Technivie GMP API supplier for your needs.
A Technivie CoA (Certificate of Analysis) is a formal document that attests to Technivie's compliance with Technivie specifications and serves as a tool for batch-level quality control.
Technivie CoA mostly includes findings from lab analyses of a specific batch. For each Technivie 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.
Technivie may be tested according to a variety of international standards, such as European Pharmacopoeia (Technivie EP), Technivie JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Technivie USP).
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