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Looking for 35554-44-0 / Enilconazole API manufacturers, exporters & distributors?

Enilconazole manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Enilconazole

Synonyms

Imazalil, 35554-44-0, Deccozil, Bromazil, Fungaflor, Imaverol

Cas Number

35554-44-0

Unique Ingredient Identifier (UNII)

6K0NOF3XQ6

Tox21_300720 Manufacturers

A Tox21_300720 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300720, including repackagers and relabelers. The FDA regulates Tox21_300720 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300720 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

Tox21_300720 Suppliers

A Tox21_300720 supplier is an individual or a company that provides Tox21_300720 active pharmaceutical ingredient (API) or Tox21_300720 finished formulations upon request. The Tox21_300720 suppliers may include Tox21_300720 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300720 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300720 CEP

A Tox21_300720 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300720 Certificate of Suitability (COS). The purpose of a Tox21_300720 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300720 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300720 to their clients by showing that a Tox21_300720 CEP has been issued for it. The manufacturer submits a Tox21_300720 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300720 CEP holder for the record. Additionally, the data presented in the Tox21_300720 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300720 DMF.

A Tox21_300720 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300720 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 Tox21_300720 suppliers with CEP (COS) on PharmaCompass.

Tox21_300720 GMP

Tox21_300720 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 Tox21_300720 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 Tox21_300720 GMP manufacturer or Tox21_300720 GMP API supplier for your needs.

Tox21_300720 CoA

A Tox21_300720 CoA (Certificate of Analysis) is a formal document that attests to Tox21_300720's compliance with Tox21_300720 specifications and serves as a tool for batch-level quality control.

Tox21_300720 CoA mostly includes findings from lab analyses of a specific batch. For each Tox21_300720 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.

Tox21_300720 may be tested according to a variety of international standards, such as European Pharmacopoeia (Tox21_300720 EP), Tox21_300720 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tox21_300720 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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