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API SUPPLIERS
Emay Pharmaceuticals is a GMP-certified API manufacturing company.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Jai Radhe Sales is your partner for all your sourcing needs.
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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USDMF
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Emay Pharmaceuticals is a GMP-certified API manufacturing company.
About the Company : Emay Pharmaceuticals Pvt Ltd functions as the merchant export division of M/s. Bhavna Laboratories Pvt Ltd. As a GMP-approved API manufacturing company, we boast over three decades...
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, ...
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...
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 ...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Fenbendazole 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 Fenbendazole manufacturer or Fenbendazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fenbendazole manufacturer or Fenbendazole supplier.
PharmaCompass also assists you with knowing the Fenbendazole API Price utilized in the formulation of products. Fenbendazole API Price is not always fixed or binding as the Fenbendazole Price is obtained through a variety of data sources. The Fenbendazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fenbendazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenbendazole, including repackagers and relabelers. The FDA regulates Fenbendazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenbendazole 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 Fenbendazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fenbendazole supplier is an individual or a company that provides Fenbendazole active pharmaceutical ingredient (API) or Fenbendazole finished formulations upon request. The Fenbendazole suppliers may include Fenbendazole API manufacturers, exporters, distributors and traders.
click here to find a list of Fenbendazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fenbendazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Fenbendazole active pharmaceutical ingredient (API) in detail. Different forms of Fenbendazole DMFs exist exist since differing nations have different regulations, such as Fenbendazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fenbendazole DMF submitted to regulatory agencies in the US is known as a USDMF. Fenbendazole USDMF includes data on Fenbendazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fenbendazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fenbendazole suppliers with USDMF on PharmaCompass.
A Fenbendazole CEP of the European Pharmacopoeia monograph is often referred to as a Fenbendazole Certificate of Suitability (COS). The purpose of a Fenbendazole CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fenbendazole EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fenbendazole to their clients by showing that a Fenbendazole CEP has been issued for it. The manufacturer submits a Fenbendazole CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fenbendazole CEP holder for the record. Additionally, the data presented in the Fenbendazole CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fenbendazole DMF.
A Fenbendazole CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fenbendazole 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 Fenbendazole suppliers with CEP (COS) 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 Fenbendazole as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fenbendazole 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 Fenbendazole 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 Fenbendazole and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fenbendazole NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fenbendazole suppliers with NDC on PharmaCompass.
Fenbendazole 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 Fenbendazole 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 Fenbendazole GMP manufacturer or Fenbendazole GMP API supplier for your needs.
A Fenbendazole CoA (Certificate of Analysis) is a formal document that attests to Fenbendazole's compliance with Fenbendazole specifications and serves as a tool for batch-level quality control.
Fenbendazole CoA mostly includes findings from lab analyses of a specific batch. For each Fenbendazole 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.
Fenbendazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Fenbendazole EP), Fenbendazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Fenbendazole USP).
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