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Looking for 130-26-7 / Clioquinol API manufacturers, exporters & distributors?

Clioquinol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Clioquinol

Synonyms

130-26-7, 5-chloro-7-iodoquinolin-8-ol, Iodochlorhydroxyquin, Chinoform, Chloroiodoquin, 5-chloro-7-iodo-8-quinolinol

Cas Number

130-26-7

Unique Ingredient Identifier (UNII)

7BHQ856EJ5

About Clioquinol

A potentially neurotoxic 8-hydroxyquinoline derivative long used as a topical anti-infective, intestinal antiamebic, and vaginal trichomonacide. The oral preparation has been shown to cause subacute myelo-optic neuropathy and has been banned worldwide.

Prestwick3_000886 Manufacturers

A Prestwick3_000886 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000886, including repackagers and relabelers. The FDA regulates Prestwick3_000886 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000886 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 Prestwick3_000886 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Prestwick3_000886 Suppliers

A Prestwick3_000886 supplier is an individual or a company that provides Prestwick3_000886 active pharmaceutical ingredient (API) or Prestwick3_000886 finished formulations upon request. The Prestwick3_000886 suppliers may include Prestwick3_000886 API manufacturers, exporters, distributors and traders.

click here to find a list of Prestwick3_000886 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Prestwick3_000886 USDMF

A Prestwick3_000886 DMF (Drug Master File) is a document detailing the whole manufacturing process of Prestwick3_000886 active pharmaceutical ingredient (API) in detail. Different forms of Prestwick3_000886 DMFs exist exist since differing nations have different regulations, such as Prestwick3_000886 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Prestwick3_000886 DMF submitted to regulatory agencies in the US is known as a USDMF. Prestwick3_000886 USDMF includes data on Prestwick3_000886's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Prestwick3_000886 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Prestwick3_000886 suppliers with USDMF on PharmaCompass.

Prestwick3_000886 WC

A Prestwick3_000886 written confirmation (Prestwick3_000886 WC) is an official document issued by a regulatory agency to a Prestwick3_000886 manufacturer, verifying that the manufacturing facility of a Prestwick3_000886 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prestwick3_000886 APIs or Prestwick3_000886 finished pharmaceutical products to another nation, regulatory agencies frequently require a Prestwick3_000886 WC (written confirmation) as part of the regulatory process.

click here to find a list of Prestwick3_000886 suppliers with Written Confirmation (WC) on PharmaCompass.

Prestwick3_000886 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 Prestwick3_000886 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Prestwick3_000886 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 Prestwick3_000886 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 Prestwick3_000886 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prestwick3_000886 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Prestwick3_000886 suppliers with NDC on PharmaCompass.

Prestwick3_000886 GMP

Prestwick3_000886 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 Prestwick3_000886 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 Prestwick3_000886 GMP manufacturer or Prestwick3_000886 GMP API supplier for your needs.

Prestwick3_000886 CoA

A Prestwick3_000886 CoA (Certificate of Analysis) is a formal document that attests to Prestwick3_000886's compliance with Prestwick3_000886 specifications and serves as a tool for batch-level quality control.

Prestwick3_000886 CoA mostly includes findings from lab analyses of a specific batch. For each Prestwick3_000886 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.

Prestwick3_000886 may be tested according to a variety of international standards, such as European Pharmacopoeia (Prestwick3_000886 EP), Prestwick3_000886 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Prestwick3_000886 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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