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1. Iodide
2. Iodides
1. Iodide
2. 20461-54-5
3. Trihydridoiodine
4. Iodide Anion
5. Iodide(1-)
6. Iodide-127
7. Iodinane
8. Iodine Anion
9. Iodide Salt
10. Lambda(3)-iodane
11. Iodide Ion(1-)
12. Iodine, Ion (i1-)
13. I-
14. Hydriodic Acid, Ion(1-)
15. 09g4i6v86q
16. 100934-04-1
17. Iodides
18. Colloidal Iodine
19. 2-propenoic Acid, 2-methyl-, Polymer With Methyl 2-methyl-2-propenoate And .alpha.-(2-methyl-1-oxo-2
20. Unii-09g4i6v86q
21. Iodide Oil
22. Iodine Ion
23. Iodine(1-)
24. Iodide Ion I-127
25. Chembl185537
26. Bdbm26981
27. Chebi:16382
28. Chebi:37181
29. Dtxsid80912339
30. Iodide (6ci,7ci,8ci,9ci)
31. Ba 2796
32. Db12754
33. C00708
34. Q407654
35. Q27117062
| Molecular Weight | 126.9045 g/mol |
|---|---|
| Molecular Formula | I- |
| XLogP3 | 0.9 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 126.90447 g/mol |
| Monoisotopic Mass | 126.90447 g/mol |
| Topological Polar Surface Area | 0 Ų |
| Heavy Atom Count | 1 |
| Formal Charge | -1 |
| Complexity | 0 |
| 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 | 1 |
API SUPPLIERS
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USDMF
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iodide, including repackagers and relabelers. The FDA regulates Iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iodide 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 Iodide supplier is an individual or a company that provides Iodide active pharmaceutical ingredient (API) or Iodide finished formulations upon request. The Iodide suppliers may include Iodide API manufacturers, exporters, distributors and traders.
click here to find a list of Iodide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iodide DMF (Drug Master File) is a document detailing the whole manufacturing process of Iodide active pharmaceutical ingredient (API) in detail. Different forms of Iodide DMFs exist exist since differing nations have different regulations, such as Iodide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iodide DMF submitted to regulatory agencies in the US is known as a USDMF. Iodide USDMF includes data on Iodide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iodide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iodide suppliers with USDMF on PharmaCompass.
Iodide 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 Iodide 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 Iodide GMP manufacturer or Iodide GMP API supplier for your needs.
A Iodide CoA (Certificate of Analysis) is a formal document that attests to Iodide's compliance with Iodide specifications and serves as a tool for batch-level quality control.
Iodide CoA mostly includes findings from lab analyses of a specific batch. For each Iodide 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.
Iodide may be tested according to a variety of international standards, such as European Pharmacopoeia (Iodide EP), Iodide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Iodide USP).
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