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1. Edurant / Truvada
2. Emtricitabine / Rilpivirine /tenofovir Disoproxil
3. Emtricitabine Mixture With Rilpivirine Hydrochloride And Tenofovir Disoproxil Fumarate
4. 847446-10-0
| Molecular Weight | 1285.6 g/mol |
|---|---|
| Molecular Formula | C53H63ClFN14O17PS |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 29 |
| Rotatable Bond Count | 26 |
| Exact Mass | 1284.3626506 g/mol |
| Monoisotopic Mass | 1284.3626506 g/mol |
| Topological Polar Surface Area | 471 Ų |
| Heavy Atom Count | 88 |
| Formal Charge | 0 |
| Complexity | 1800 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 5 |
| 1 of 2 | |
|---|---|
| Drug Name | Complera |
| PubMed Health | Emtricitabine/Rilpivirine/Tenofovir (By mouth) |
| Drug Classes | Antiretroviral Agent |
| Drug Label | COMPLERA is a fixed-dose combination tablet containing emtricitabine, rilpivirine hydrochloride, and tenofovir DF. EMTRIVA is the brand name for emtricitabine, a synthetic nucleoside analog of cytidine. EDURANT is the brand name for rilpivirine, a no... |
| Active Ingredient | tenofovir disoproxil fumarate; rilpivirine hydrochloride; Emtricitabine |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 300mg; 200mg; eq 25mg base |
| Market Status | Prescription |
| Company | Gilead Sciences |
| 2 of 2 | |
|---|---|
| Drug Name | Complera |
| PubMed Health | Emtricitabine/Rilpivirine/Tenofovir (By mouth) |
| Drug Classes | Antiretroviral Agent |
| Drug Label | COMPLERA is a fixed-dose combination tablet containing emtricitabine, rilpivirine hydrochloride, and tenofovir DF. EMTRIVA is the brand name for emtricitabine, a synthetic nucleoside analog of cytidine. EDURANT is the brand name for rilpivirine, a no... |
| Active Ingredient | tenofovir disoproxil fumarate; rilpivirine hydrochloride; Emtricitabine |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 300mg; 200mg; eq 25mg base |
| Market Status | Prescription |
| Company | Gilead Sciences |
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ABOUT THIS PAGE
A Edurant / Truvada manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edurant / Truvada, including repackagers and relabelers. The FDA regulates Edurant / Truvada manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Edurant / Truvada 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 Edurant / Truvada supplier is an individual or a company that provides Edurant / Truvada active pharmaceutical ingredient (API) or Edurant / Truvada finished formulations upon request. The Edurant / Truvada suppliers may include Edurant / Truvada API manufacturers, exporters, distributors and traders.
Edurant / Truvada 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 Edurant / Truvada 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 Edurant / Truvada GMP manufacturer or Edurant / Truvada GMP API supplier for your needs.
A Edurant / Truvada CoA (Certificate of Analysis) is a formal document that attests to Edurant / Truvada's compliance with Edurant / Truvada specifications and serves as a tool for batch-level quality control.
Edurant / Truvada CoA mostly includes findings from lab analyses of a specific batch. For each Edurant / Truvada 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.
Edurant / Truvada may be tested according to a variety of international standards, such as European Pharmacopoeia (Edurant / Truvada EP), Edurant / Truvada JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Edurant / Truvada USP).
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