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API SUPPLIERS
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USDMF
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IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
About the Company : Established in 1990, Inabata France, a part of the Inabata Group, used to export chemical and pharmaceutical products to Japan. In 2006, it acquired Pharmasynthèse. Today, Inabata...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
About the Company : Gonane Pharma, is a contract pharmaceutical company located in Gujarat, India, specializing in the manufacturing and marketing of Corticosteroids, Hormones, Antivirals, and Oncolog...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
About the Company : PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipients for pharmaceuti...
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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.
A Lomexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomexin, including repackagers and relabelers. The FDA regulates Lomexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomexin 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 Lomexin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lomexin supplier is an individual or a company that provides Lomexin active pharmaceutical ingredient (API) or Lomexin finished formulations upon request. The Lomexin suppliers may include Lomexin API manufacturers, exporters, distributors and traders.
click here to find a list of Lomexin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lomexin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lomexin active pharmaceutical ingredient (API) in detail. Different forms of Lomexin DMFs exist exist since differing nations have different regulations, such as Lomexin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lomexin DMF submitted to regulatory agencies in the US is known as a USDMF. Lomexin USDMF includes data on Lomexin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lomexin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lomexin suppliers with USDMF on PharmaCompass.
A Lomexin CEP of the European Pharmacopoeia monograph is often referred to as a Lomexin Certificate of Suitability (COS). The purpose of a Lomexin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lomexin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lomexin to their clients by showing that a Lomexin CEP has been issued for it. The manufacturer submits a Lomexin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lomexin CEP holder for the record. Additionally, the data presented in the Lomexin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lomexin DMF.
A Lomexin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lomexin 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 Lomexin suppliers with CEP (COS) on PharmaCompass.
A Lomexin written confirmation (Lomexin WC) is an official document issued by a regulatory agency to a Lomexin manufacturer, verifying that the manufacturing facility of a Lomexin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lomexin APIs or Lomexin finished pharmaceutical products to another nation, regulatory agencies frequently require a Lomexin WC (written confirmation) as part of the regulatory process.
click here to find a list of Lomexin suppliers with Written Confirmation (WC) on PharmaCompass.
Lomexin 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 Lomexin 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 Lomexin GMP manufacturer or Lomexin GMP API supplier for your needs.
A Lomexin CoA (Certificate of Analysis) is a formal document that attests to Lomexin's compliance with Lomexin specifications and serves as a tool for batch-level quality control.
Lomexin CoA mostly includes findings from lab analyses of a specific batch. For each Lomexin 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.
Lomexin may be tested according to a variety of international standards, such as European Pharmacopoeia (Lomexin EP), Lomexin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lomexin USP).
