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Looking for 7681-82-5 / Sodium Iodide API manufacturers, exporters & distributors?

Sodium Iodide manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sodium Iodide

Synonyms

7681-82-5, Ioduril, Sodium monoiodide, Soiodin, Iodure de sodium, Sodium iodide (nai)

Cas Number

7681-82-5

Unique Ingredient Identifier (UNII)

F5WR8N145C

About Sodium Iodide

A compound forming white, odorless deliquescent crystals and used as iodine supplement, expectorant or in its radioactive (I-131) form as an diagnostic aid, particularly for thyroid function tests.

Sodium iodide I 123 Manufacturers

A Sodium iodide I 123 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium iodide I 123, including repackagers and relabelers. The FDA regulates Sodium iodide I 123 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium iodide I 123 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 Sodium iodide I 123 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Sodium iodide I 123 Suppliers

A Sodium iodide I 123 supplier is an individual or a company that provides Sodium iodide I 123 active pharmaceutical ingredient (API) or Sodium iodide I 123 finished formulations upon request. The Sodium iodide I 123 suppliers may include Sodium iodide I 123 API manufacturers, exporters, distributors and traders.

click here to find a list of Sodium iodide I 123 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Sodium iodide I 123 USDMF

A Sodium iodide I 123 DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium iodide I 123 active pharmaceutical ingredient (API) in detail. Different forms of Sodium iodide I 123 DMFs exist exist since differing nations have different regulations, such as Sodium iodide I 123 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Sodium iodide I 123 DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium iodide I 123 USDMF includes data on Sodium iodide I 123's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium iodide I 123 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Sodium iodide I 123 suppliers with USDMF on PharmaCompass.

Sodium iodide I 123 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 Sodium iodide I 123 Drug Master File in Japan (Sodium iodide I 123 JDMF) empowers Sodium iodide I 123 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 Sodium iodide I 123 JDMF during the approval evaluation for pharmaceutical products. At the time of Sodium iodide I 123 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 Sodium iodide I 123 suppliers with JDMF on PharmaCompass.

Sodium iodide I 123 WC

A Sodium iodide I 123 written confirmation (Sodium iodide I 123 WC) is an official document issued by a regulatory agency to a Sodium iodide I 123 manufacturer, verifying that the manufacturing facility of a Sodium iodide I 123 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sodium iodide I 123 APIs or Sodium iodide I 123 finished pharmaceutical products to another nation, regulatory agencies frequently require a Sodium iodide I 123 WC (written confirmation) as part of the regulatory process.

click here to find a list of Sodium iodide I 123 suppliers with Written Confirmation (WC) on PharmaCompass.

Sodium iodide I 123 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 Sodium iodide I 123 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Sodium iodide I 123 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 Sodium iodide I 123 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 Sodium iodide I 123 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium iodide I 123 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Sodium iodide I 123 suppliers with NDC on PharmaCompass.

Sodium iodide I 123 GMP

Sodium iodide I 123 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 iodide I 123 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 iodide I 123 GMP manufacturer or Sodium iodide I 123 GMP API supplier for your needs.

Sodium iodide I 123 CoA

A Sodium iodide I 123 CoA (Certificate of Analysis) is a formal document that attests to Sodium iodide I 123's compliance with Sodium iodide I 123 specifications and serves as a tool for batch-level quality control.

Sodium iodide I 123 CoA mostly includes findings from lab analyses of a specific batch. For each Sodium iodide I 123 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 iodide I 123 may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium iodide I 123 EP), Sodium iodide I 123 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium iodide I 123 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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