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Looking for 7681-11-0 / Potassium Iodide API manufacturers, exporters & distributors?

Potassium Iodide manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Potassium Iodide 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 Potassium Iodide manufacturer or Potassium Iodide supplier for your needs.

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

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

API | Excipient name

Potassium Iodide

Synonyms

7681-11-0, Thyro-block, Pima, Kali iodide, Potassium iodide (ki), Knollide

Cas Number

7681-11-0

Unique Ingredient Identifier (UNII)

1C4QK22F9J

About Potassium Iodide

An inorganic compound that is used as a source of iodine in thyrotoxic crisis and in the preparation of thyrotoxic patients for thyroidectomy. (From Dorland, 27th ed)

03124_RIEDEL Manufacturers

A 03124_RIEDEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03124_RIEDEL, including repackagers and relabelers. The FDA regulates 03124_RIEDEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03124_RIEDEL 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 03124_RIEDEL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

03124_RIEDEL Suppliers

A 03124_RIEDEL supplier is an individual or a company that provides 03124_RIEDEL active pharmaceutical ingredient (API) or 03124_RIEDEL finished formulations upon request. The 03124_RIEDEL suppliers may include 03124_RIEDEL API manufacturers, exporters, distributors and traders.

click here to find a list of 03124_RIEDEL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

03124_RIEDEL USDMF

A 03124_RIEDEL DMF (Drug Master File) is a document detailing the whole manufacturing process of 03124_RIEDEL active pharmaceutical ingredient (API) in detail. Different forms of 03124_RIEDEL DMFs exist exist since differing nations have different regulations, such as 03124_RIEDEL USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 03124_RIEDEL DMF submitted to regulatory agencies in the US is known as a USDMF. 03124_RIEDEL USDMF includes data on 03124_RIEDEL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 03124_RIEDEL USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 03124_RIEDEL suppliers with USDMF on PharmaCompass.

03124_RIEDEL JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The 03124_RIEDEL Drug Master File in Japan (03124_RIEDEL JDMF) empowers 03124_RIEDEL API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the 03124_RIEDEL JDMF during the approval evaluation for pharmaceutical products. At the time of 03124_RIEDEL JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of 03124_RIEDEL suppliers with JDMF on PharmaCompass.

03124_RIEDEL CEP

A 03124_RIEDEL CEP of the European Pharmacopoeia monograph is often referred to as a 03124_RIEDEL Certificate of Suitability (COS). The purpose of a 03124_RIEDEL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 03124_RIEDEL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 03124_RIEDEL to their clients by showing that a 03124_RIEDEL CEP has been issued for it. The manufacturer submits a 03124_RIEDEL CEP (COS) as part of the market authorization procedure, and it takes on the role of a 03124_RIEDEL CEP holder for the record. Additionally, the data presented in the 03124_RIEDEL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 03124_RIEDEL DMF.

A 03124_RIEDEL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 03124_RIEDEL CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

click here to find a list of 03124_RIEDEL suppliers with CEP (COS) on PharmaCompass.

03124_RIEDEL WC

A 03124_RIEDEL written confirmation (03124_RIEDEL WC) is an official document issued by a regulatory agency to a 03124_RIEDEL manufacturer, verifying that the manufacturing facility of a 03124_RIEDEL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 03124_RIEDEL APIs or 03124_RIEDEL finished pharmaceutical products to another nation, regulatory agencies frequently require a 03124_RIEDEL WC (written confirmation) as part of the regulatory process.

click here to find a list of 03124_RIEDEL suppliers with Written Confirmation (WC) on PharmaCompass.

03124_RIEDEL NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing 03124_RIEDEL as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 03124_RIEDEL API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture 03124_RIEDEL as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain 03124_RIEDEL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 03124_RIEDEL NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 03124_RIEDEL suppliers with NDC on PharmaCompass.

03124_RIEDEL GMP

03124_RIEDEL 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 03124_RIEDEL 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 03124_RIEDEL GMP manufacturer or 03124_RIEDEL GMP API supplier for your needs.

03124_RIEDEL CoA

A 03124_RIEDEL CoA (Certificate of Analysis) is a formal document that attests to 03124_RIEDEL's compliance with 03124_RIEDEL specifications and serves as a tool for batch-level quality control.

03124_RIEDEL CoA mostly includes findings from lab analyses of a specific batch. For each 03124_RIEDEL 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.

03124_RIEDEL may be tested according to a variety of international standards, such as European Pharmacopoeia (03124_RIEDEL EP), 03124_RIEDEL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (03124_RIEDEL 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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