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Looking for 73151-29-8 / Fenticonazole Nitrate API manufacturers, exporters & distributors?

Fenticonazole Nitrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Fenticonazole Nitrate

Synonyms

73151-29-8, Lomexin, Falvin, Fenticonazole mononitrate, Fenticonazole (nitrate), Rec 15/1476

Cas Number

73151-29-8

Unique Ingredient Identifier (UNII)

8V4JGC8YRF

Fenticonazole Manufacturers

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

Fenticonazole Suppliers

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

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

Fenticonazole USDMF

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

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

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

Fenticonazole CEP

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

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

Fenticonazole WC

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

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

Fenticonazole GMP

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

Fenticonazole CoA

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

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

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