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  • INJECTABLE;INJECTION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • CAPSULE, EXTENDED RELEASE;ORAL - 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • CAPSULE, EXTENDED RELEASE;ORAL - 8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • TABLET, EXTENDED RELEASE;ORAL - 8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;450MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;224MG/100ML;450MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;450MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;450MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;225MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • SOLUTION;IRRIGATION - 0.154MG/ML;0.92MG/ML;0.184MG/ML;0.2MG/ML;0.38MG/ML;2.1MG/ML;7.14MG/ML;0.42MG/ML
  • TABLET, EXTENDED RELEASE;ORAL - 10MEQ
  • TABLET, EXTENDED RELEASE;ORAL - 8MEQ
  • SOLUTION;IRRIGATION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;104MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;328MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;149MG/100ML;900MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;224MG/100ML;900MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;900MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;900MG/100ML
  • FOR SOLUTION;ORAL - 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT
  • INJECTABLE;INJECTION - 1.49GM/100ML
  • INJECTABLE;INJECTION - 14.9MG/ML
  • INJECTABLE;INJECTION - 2.24GM/100ML
  • INJECTABLE;INJECTION - 2.98GM/100ML
  • INJECTABLE;INJECTION - 29.8MG/ML
  • INJECTABLE;INJECTION - 745MG/100ML
  • INJECTABLE;INJECTION - 3.68GM/1000ML;3.05GM/1000ML;0.314GM/1000ML ;3.09GM/1000ML;6.34GM/1000ML;0.187GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;6.95GM/1000ML;0.187GM/1000ML (5000ML)
  • SOLUTION;IRRIGATION - 0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML
  • FOR SOLUTION;ORAL - 10MEQ
  • FOR SOLUTION;ORAL - 20MEQ
  • FOR SOLUTION;ORAL - 40MEQ
  • INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - 3.68GM/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - 5.15GM/1000ML;20GM/1000ML;5.4GM/1000ML;2.03GM/1000ML;0.157GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - 5.15GM/1000ML;N/A/1000ML;5.4GM/1000ML;2.03GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;2.03GM/1000ML;0.157GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;2.44GM/1000ML;0.314GM/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.157GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;20GM/1000ML;5.4GM/1000ML;3.05GM/1000ML;0.314GM/1000ML;2.21GM/1000ML;7.07GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - N/A/1000ML;N/A/1000ML;5.4GM/1000ML;2.44GM/1000ML;N/A/1000ML;3.09GM/1000ML;6.46GM/1000ML (5000ML)
  • INJECTABLE;INJECTION - 2MEQ/ML

Looking for 7447-40-7 / Potassium Chloride API manufacturers, exporters & distributors?

Potassium Chloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Potassium Chloride

Synonyms

7447-40-7, Sylvite, Klotrix, Enseal, Slow-k, Klor-con

Cas Number

7447-40-7

Unique Ingredient Identifier (UNII)

660YQ98I10

About Potassium Chloride

A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.

Potassium Chloride API Manufacturers

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

Potassium Chloride API Suppliers

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

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

Potassium Chloride API USDMF

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

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

click here to find a list of Potassium Chloride API suppliers with USDMF on PharmaCompass.

Potassium Chloride API 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 Potassium Chloride API Drug Master File in Japan (Potassium Chloride API JDMF) empowers Potassium Chloride API 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 Potassium Chloride API JDMF during the approval evaluation for pharmaceutical products. At the time of Potassium Chloride API 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 Potassium Chloride API suppliers with JDMF on PharmaCompass.

Potassium Chloride API KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Potassium Chloride API Drug Master File in Korea (Potassium Chloride API KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Potassium Chloride API. The MFDS reviews the Potassium Chloride API KDMF as part of the drug registration process and uses the information provided in the Potassium Chloride API KDMF to evaluate the safety and efficacy of the drug.

After submitting a Potassium Chloride API KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Potassium Chloride API API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Potassium Chloride API suppliers with KDMF on PharmaCompass.

Potassium Chloride API CEP

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

A Potassium Chloride API CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Potassium Chloride API 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 Potassium Chloride API suppliers with CEP (COS) on PharmaCompass.

Potassium Chloride API WC

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

click here to find a list of Potassium Chloride API suppliers with Written Confirmation (WC) on PharmaCompass.

Potassium Chloride API 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 Potassium Chloride API as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Potassium Chloride API suppliers with NDC on PharmaCompass.

Potassium Chloride API GMP

Potassium Chloride API 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 Chloride API 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 Chloride API GMP manufacturer or Potassium Chloride API GMP API supplier for your needs.

Potassium Chloride API CoA

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

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