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API SUPPLIERS
Suanfarma, at the Core of a Better Life.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Temad- We think of world-class quality.
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EU WC
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ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
VMF Number : 5974
Submission : 2009-12-29
Status :
Type : II
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Listed Suppliers
Suanfarma, at the Core of a Better Life.
About the Company : Suanfarma founded in 1993, is a B2B life science partner committed to health & innovation by developing, manufacturing, & distributing high-quality APIs for the pharmaceutical indu...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
Temad- We think of world-class quality.
About the Company : Established in 1997, Temad Co. is one of the largest producers of APIs in Iran & an innovative manufacturer of narcotic and non-narcotic products of world-class quality in the Midd...
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ABOUT THIS PAGE
A Florfenicol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Florfenicol, including repackagers and relabelers. The FDA regulates Florfenicol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Florfenicol 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 Florfenicol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Florfenicol supplier is an individual or a company that provides Florfenicol active pharmaceutical ingredient (API) or Florfenicol finished formulations upon request. The Florfenicol suppliers may include Florfenicol API manufacturers, exporters, distributors and traders.
click here to find a list of Florfenicol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Florfenicol written confirmation (Florfenicol WC) is an official document issued by a regulatory agency to a Florfenicol manufacturer, verifying that the manufacturing facility of a Florfenicol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Florfenicol APIs or Florfenicol finished pharmaceutical products to another nation, regulatory agencies frequently require a Florfenicol WC (written confirmation) as part of the regulatory process.
click here to find a list of Florfenicol suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Florfenicol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Florfenicol API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Florfenicol as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Florfenicol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Florfenicol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Florfenicol suppliers with NDC on PharmaCompass.
Florfenicol 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 Florfenicol 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 Florfenicol GMP manufacturer or Florfenicol GMP API supplier for your needs.
A Florfenicol CoA (Certificate of Analysis) is a formal document that attests to Florfenicol's compliance with Florfenicol specifications and serves as a tool for batch-level quality control.
Florfenicol CoA mostly includes findings from lab analyses of a specific batch. For each Florfenicol 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.
Florfenicol may be tested according to a variety of international standards, such as European Pharmacopoeia (Florfenicol EP), Florfenicol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Florfenicol USP).
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