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Looking for 2127-01-7 / Clorexolone API manufacturers, exporters & distributors?

Clorexolone manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Clorexolone

Synonyms

Chlorexolone, 2127-01-7, Clorexolon, Flonatril, Nefrolan, Klorex

Cas Number

2127-01-7

Unique Ingredient Identifier (UNII)

Q2PLT3FS05

About Clorexolone

Clorexolone is a sulfonamide-based diuretic with thiazide-like activity. Cloreloxone has actions similar to that of thiazide diuretics.

Clorexolone Manufacturers

A Clorexolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clorexolone, including repackagers and relabelers. The FDA regulates Clorexolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clorexolone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Clorexolone Suppliers

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

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

Clorexolone USDMF

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

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

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

Clorexolone GMP

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

Clorexolone CoA

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

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

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