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Looking for 14038-43-8 / Ferric Ferrocyanide API manufacturers, exporters & distributors?

Ferric Ferrocyanide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ferric Ferrocyanide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Ferric Ferrocyanide manufacturer or Ferric Ferrocyanide supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferric Ferrocyanide manufacturer or Ferric Ferrocyanide supplier.

PharmaCompass also assists you with knowing the Ferric Ferrocyanide API Price utilized in the formulation of products. Ferric Ferrocyanide API Price is not always fixed or binding as the Ferric Ferrocyanide Price is obtained through a variety of data sources. The Ferric Ferrocyanide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Ferric Ferrocyanide

Synonyms

Iron(iii) hexacyanoferrate(ii), Prussian blue insoluble, Iron(2+);iron(3+);octadecacyanide, Iron(iii) ferrocyanide; milori blue, Ferrocin, Parisian blue

Cas Number

14038-43-8

About Ferric Ferrocyanide

Prussian blue is described as a deep blue pigment that is produced when the oxidation of ferrous ferrocyanide salts occurs. It contains ferric hexacyanoferrate(II) in a cubic lattice crystal structure. It is insoluble in water but also tends to form a colloid thus can exist in either colloidal or water-soluble form, and an insoluble form. It is orally administered for clinical purposes to be used as an antidote for certain kinds of heavy metal poisoning, such as thallium and radioactive isotopes of caesium. Prussian blue is included in the World Health Organization Model List of Essential Medicines as a specific antidote used in poisonings to provide symptomatic and supportive treatment. It was also administered in individuals exposed to 137-Cs+ during Goinia accident, one of the worst radioactive contamination incidents that occured in Brazil, 1983.

Preussischblau Manufacturers

A Preussischblau manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Preussischblau, including repackagers and relabelers. The FDA regulates Preussischblau manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Preussischblau API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Preussischblau Suppliers

A Preussischblau supplier is an individual or a company that provides Preussischblau active pharmaceutical ingredient (API) or Preussischblau finished formulations upon request. The Preussischblau suppliers may include Preussischblau API manufacturers, exporters, distributors and traders.

Preussischblau GMP

Preussischblau 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 Preussischblau 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 Preussischblau GMP manufacturer or Preussischblau GMP API supplier for your needs.

Preussischblau CoA

A Preussischblau CoA (Certificate of Analysis) is a formal document that attests to Preussischblau's compliance with Preussischblau specifications and serves as a tool for batch-level quality control.

Preussischblau CoA mostly includes findings from lab analyses of a specific batch. For each Preussischblau 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.

Preussischblau may be tested according to a variety of international standards, such as European Pharmacopoeia (Preussischblau EP), Preussischblau JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Preussischblau USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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