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Looking for 101-20-2 / Triclocarban API manufacturers, exporters & distributors?

Triclocarban manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Triclocarban

Synonyms

101-20-2, 1-(4-chlorophenyl)-3-(3,4-dichlorophenyl)urea, 3,4,4'-trichlorocarbanilide, Solubacter, Cutisan, Procutene

Cas Number

101-20-2

Unique Ingredient Identifier (UNII)

BGG1Y1ED0Y

About Triclocarban

Triclocarban is a triclosan analogue with an antibacterial property. Triclocarban exerts its effect by inhibiting the activity of enoyl-(acyl-carrier protein) (ACP) reductase, widely distributed in bacteria, fungi and plants. ACP reductase catalyses the last step in each cycle of fatty acid elongation in the type II fatty acid synthase systems. As a result, this agent interrupts cell membrane synthesis and leads to bacterial growth inhibition.

MolPort-001-012-487 Manufacturers

A MolPort-001-012-487 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-012-487, including repackagers and relabelers. The FDA regulates MolPort-001-012-487 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-012-487 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

MolPort-001-012-487 Suppliers

A MolPort-001-012-487 supplier is an individual or a company that provides MolPort-001-012-487 active pharmaceutical ingredient (API) or MolPort-001-012-487 finished formulations upon request. The MolPort-001-012-487 suppliers may include MolPort-001-012-487 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-012-487 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-012-487 USDMF

A MolPort-001-012-487 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-012-487 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-012-487 DMFs exist exist since differing nations have different regulations, such as MolPort-001-012-487 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MolPort-001-012-487 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-012-487 USDMF includes data on MolPort-001-012-487's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-012-487 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MolPort-001-012-487 suppliers with USDMF on PharmaCompass.

MolPort-001-012-487 GMP

MolPort-001-012-487 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 MolPort-001-012-487 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 MolPort-001-012-487 GMP manufacturer or MolPort-001-012-487 GMP API supplier for your needs.

MolPort-001-012-487 CoA

A MolPort-001-012-487 CoA (Certificate of Analysis) is a formal document that attests to MolPort-001-012-487's compliance with MolPort-001-012-487 specifications and serves as a tool for batch-level quality control.

MolPort-001-012-487 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-001-012-487 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.

MolPort-001-012-487 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-001-012-487 EP), MolPort-001-012-487 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-001-012-487 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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