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  • INJECTABLE;INJECTION - 900MG/100ML
  • SOLUTION;INJECTION - 225MG/25ML (9MG/ML)
  • SOLUTION;INJECTION - 450MG/50ML (9MG/ML)
  • SOLUTION;INJECTION - 900MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • SOLUTION;IRRIGATION - 900MG/100ML
  • SOLUTION;IRRIGATION - 900MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;900MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;225MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;450MG/100ML
  • INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 5GM/100ML;300MG/100ML
  • INJECTABLE;INJECTION - 450MG/100ML
  • INJECTABLE;INJECTION - 450MG/100ML
  • 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- 5GM/100ML;298MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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- 5GM/100ML;74.5MG/100ML;225MG/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
  • SOLUTION;INJECTION - 180MG/20ML (9MG/ML)
  • SOLUTION;INJECTION - 270MG/30ML (9MG/ML)
  • SOLUTION;INJECTION - 90MG/10ML (9MG/ML)
  • SOLUTION;INJECTION - 180MG/20ML (9MG/ML)
  • SOLUTION;INJECTION - 18MG/2ML (9MG/ML)
  • SOLUTION;INJECTION - 27MG/3ML (9MG/ML)
  • SOLUTION;INJECTION - 450MG/50ML (9MG/ML)
  • SOLUTION;INJECTION - 45MG/5ML (9MG/ML)
  • SOLUTION;INJECTION - 90MG/10ML (9MG/ML)
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;15.2MG/100ML;567MG/100ML;392MG/100ML
  • SOLUTION;INTRAPERITONEAL - 25.7MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML
  • SOLUTION;IRRIGATION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
  • INJECTABLE;INJECTION - 450MG/100ML
  • INJECTABLE;INJECTION - 900MG/100ML
  • SOLUTION;INJECTION - 90MG/10ML (9MG/ML)
  • 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
  • SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;1.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML
  • SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;2.5GM/100ML;5.08MG/100ML;538MG/100ML;448MG/100ML
  • SOLUTION;INTRAPERITONEAL - 18.4MG/100ML;4.25GM/100ML;5.08MG/100ML;538MG/100ML;448MG/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
  • 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)

Looking for 7647-14-5 / Sodium Chloride API manufacturers, exporters & distributors?

Sodium Chloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sodium Chloride

Synonyms

7647-14-5, Salt, Table salt, Halite, Saline, Rock salt

Cas Number

7647-14-5

Unique Ingredient Identifier (UNII)

451W47IQ8X

About Sodium Chloride

A ubiquitous sodium salt that is commonly used to season food.

03370_FLUKA Manufacturers

A 03370_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03370_FLUKA, including repackagers and relabelers. The FDA regulates 03370_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03370_FLUKA 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 03370_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

03370_FLUKA Suppliers

A 03370_FLUKA supplier is an individual or a company that provides 03370_FLUKA active pharmaceutical ingredient (API) or 03370_FLUKA finished formulations upon request. The 03370_FLUKA suppliers may include 03370_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 03370_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

03370_FLUKA USDMF

A 03370_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 03370_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 03370_FLUKA DMFs exist exist since differing nations have different regulations, such as 03370_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 03370_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 03370_FLUKA USDMF includes data on 03370_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 03370_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 03370_FLUKA suppliers with USDMF on PharmaCompass.

03370_FLUKA 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 03370_FLUKA Drug Master File in Japan (03370_FLUKA JDMF) empowers 03370_FLUKA 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 03370_FLUKA JDMF during the approval evaluation for pharmaceutical products. At the time of 03370_FLUKA 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 03370_FLUKA suppliers with JDMF on PharmaCompass.

03370_FLUKA KDMF

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

Pharmaceutical companies submit a 03370_FLUKA Drug Master File in Korea (03370_FLUKA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 03370_FLUKA. The MFDS reviews the 03370_FLUKA KDMF as part of the drug registration process and uses the information provided in the 03370_FLUKA KDMF to evaluate the safety and efficacy of the drug.

After submitting a 03370_FLUKA 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 03370_FLUKA API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 03370_FLUKA suppliers with KDMF on PharmaCompass.

03370_FLUKA CEP

A 03370_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 03370_FLUKA Certificate of Suitability (COS). The purpose of a 03370_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 03370_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 03370_FLUKA to their clients by showing that a 03370_FLUKA CEP has been issued for it. The manufacturer submits a 03370_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 03370_FLUKA CEP holder for the record. Additionally, the data presented in the 03370_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 03370_FLUKA DMF.

A 03370_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 03370_FLUKA 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 03370_FLUKA suppliers with CEP (COS) on PharmaCompass.

03370_FLUKA WC

A 03370_FLUKA written confirmation (03370_FLUKA WC) is an official document issued by a regulatory agency to a 03370_FLUKA manufacturer, verifying that the manufacturing facility of a 03370_FLUKA active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 03370_FLUKA APIs or 03370_FLUKA finished pharmaceutical products to another nation, regulatory agencies frequently require a 03370_FLUKA WC (written confirmation) as part of the regulatory process.

click here to find a list of 03370_FLUKA suppliers with Written Confirmation (WC) on PharmaCompass.

03370_FLUKA 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 03370_FLUKA as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 03370_FLUKA 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 03370_FLUKA 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 03370_FLUKA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 03370_FLUKA NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 03370_FLUKA suppliers with NDC on PharmaCompass.

03370_FLUKA GMP

03370_FLUKA 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 03370_FLUKA 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 03370_FLUKA GMP manufacturer or 03370_FLUKA GMP API supplier for your needs.

03370_FLUKA CoA

A 03370_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 03370_FLUKA's compliance with 03370_FLUKA specifications and serves as a tool for batch-level quality control.

03370_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 03370_FLUKA 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.

03370_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (03370_FLUKA EP), 03370_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (03370_FLUKA 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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