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1. 13472-33-8
2. Sodium;oxido(trioxo)rhenium
3. Rhenate (reo41-), Sodium, (t-4)-
4. Pe1t8nn47q
5. Rhenate (reo41-), Sodium (1:1), (t-4)-
6. Mfcd00014231
7. Rhenium(vii) Sodium Oxide
8. Unii-pe1t8nn47q
9. Sodium Tetraoxorhenate(1-)
10. Einecs 236-742-9
11. Perrhenic Acid (hreo4), Sodium Salt
12. Perrhenic Acid Sodium Salt
13. Ec 236-742-9
14. Sodium Perrhenate (nareo4)
15. Perrhenic Acid(hreo4), Sodium Salt
16. Akos015910781
17. Rhenium Sodium Oxide (renao4)
18. Rhenate(reo4(sup 1-)), Sodium, (t-4)-
19. Q2592158
| Molecular Weight | 273.19 g/mol |
|---|---|
| Molecular Formula | NaO4Re |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 273.925180 g/mol |
| Monoisotopic Mass | 273.925180 g/mol |
| Topological Polar Surface Area | 74.3 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 118 |
| 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 Sodium Perrhenate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Perrhenate, including repackagers and relabelers. The FDA regulates Sodium Perrhenate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Perrhenate 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 Sodium Perrhenate supplier is an individual or a company that provides Sodium Perrhenate active pharmaceutical ingredient (API) or Sodium Perrhenate finished formulations upon request. The Sodium Perrhenate suppliers may include Sodium Perrhenate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Perrhenate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Perrhenate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Perrhenate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Perrhenate DMFs exist exist since differing nations have different regulations, such as Sodium Perrhenate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Perrhenate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Perrhenate USDMF includes data on Sodium Perrhenate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Perrhenate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Perrhenate suppliers with USDMF on PharmaCompass.
Sodium Perrhenate 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 Sodium Perrhenate 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 Sodium Perrhenate GMP manufacturer or Sodium Perrhenate GMP API supplier for your needs.
A Sodium Perrhenate CoA (Certificate of Analysis) is a formal document that attests to Sodium Perrhenate's compliance with Sodium Perrhenate specifications and serves as a tool for batch-level quality control.
Sodium Perrhenate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Perrhenate 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.
Sodium Perrhenate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Perrhenate EP), Sodium Perrhenate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Perrhenate USP).
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