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1. 7758-05-6
2. Potassium Triodate
3. Iodic Acid, Potassium Salt
4. Iodic Acid (hio3), Potassium Salt
5. I139e44nhl
6. Mfcd00011406
7. Potassiumiodate
8. Caswell No. 693a
9. Kaliumjodat
10. Potassium;iodate
11. Hsdb 1231
12. Einecs 231-831-9
13. Epa Pesticide Chemical Code 075703
14. Nsc 215201
15. Unii-i139e44nhl
16. Potassium Iodate, Acs Grade
17. Potassium Iodate [mi]
18. Potassium Iodate(v) (kio3)
19. Potassium Iodate [fcc]
20. Potassium Iodate [hsdb]
21. Dtxsid5058480
22. Potassium Iodate [mart.]
23. Potassium Iodate [who-dd]
24. Akos015853994
25. Iodic Acid (hio3), Potassium Salt (1:1)
26. Potassium Iodate, 0.1n Standardized Solution
27. Ec 231-831-9
28. Iodic Acid (hio3) Potassium Salt (1:1)
29. Q414599
| Molecular Weight | 214.001 g/mol |
|---|---|
| Molecular Formula | IKO3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 213.85292 g/mol |
| Monoisotopic Mass | 213.85292 g/mol |
| Topological Polar Surface Area | 57.2 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 49.8 |
| 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 |
Antifungal Agents
National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)
EXPTL USE: TO PREVENT 131(I) UPTAKE BY THE THYROID DURING CISTERNOGRAPHY WITH 131(I)-LABELED SERUM ALBUMIN, PT WERE GIVEN IN ADVANCE TABLETS CONTAINING 85 MG POTASSIUM IODATE.
VAN DE POLL MA P ET AL; PHARM WEEKBL 111(12) 252 (1976)
HAS BEEN USED AS A TOPICAL ANTISEPTIC FOR MUCOUS MEMBRANE INFECTIONS. DOSE: TOPICALLY 0.5% SOLN.
The Merck Index: An Encyclopedia of Chemicals and Drugs 8th ed. Rahway, New Jersey: Merck and Co., Inc., 1968., p. 855
MEDICATION (VET): IN FEEDS AS A SOURCE OF IODINE
The Merck Index. 9th ed. Rahway, New Jersey: Merck & Co., Inc., 1976., p. 992
4. 4= VERY TOXIC: PROBABLE ORAL LETHAL DOSE (HUMAN) 50-500 MG/KG, BETWEEN 1 TEASPOON & 1 OUNCE FOR 70 KG PERSON (150 LB).
Gosselin, R.E., H.C. Hodge, R.P. Smith, and M.N. Gleason. Clinical Toxicology of Commercial Products. 4th ed. Baltimore: Williams and Wilkins, 1976., p. II-77
Antifungal Agents
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)
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ABOUT THIS PAGE
A Potassium Iodate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potassium Iodate, including repackagers and relabelers. The FDA regulates Potassium Iodate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potassium Iodate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Potassium Iodate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Potassium Iodate supplier is an individual or a company that provides Potassium Iodate active pharmaceutical ingredient (API) or Potassium Iodate finished formulations upon request. The Potassium Iodate suppliers may include Potassium Iodate API manufacturers, exporters, distributors and traders.
click here to find a list of Potassium Iodate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Potassium Iodate written confirmation (Potassium Iodate WC) is an official document issued by a regulatory agency to a Potassium Iodate manufacturer, verifying that the manufacturing facility of a Potassium Iodate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Potassium Iodate APIs or Potassium Iodate finished pharmaceutical products to another nation, regulatory agencies frequently require a Potassium Iodate WC (written confirmation) as part of the regulatory process.
click here to find a list of Potassium Iodate suppliers with Written Confirmation (WC) on PharmaCompass.
Potassium Iodate 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 Potassium Iodate 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 Potassium Iodate GMP manufacturer or Potassium Iodate GMP API supplier for your needs.
A Potassium Iodate CoA (Certificate of Analysis) is a formal document that attests to Potassium Iodate's compliance with Potassium Iodate specifications and serves as a tool for batch-level quality control.
Potassium Iodate CoA mostly includes findings from lab analyses of a specific batch. For each Potassium Iodate 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.
Potassium Iodate may be tested according to a variety of international standards, such as European Pharmacopoeia (Potassium Iodate EP), Potassium Iodate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Potassium Iodate USP).
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