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API SUPPLIERS
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USDMF
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Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
About the Company : Symbiotec, a leading API manufacturing company based in Indore, Central India, specializes in Cortico-Steroids and Steroid-Hormone APIs. Since 1995, their focus on R&D, sustainable...
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...
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Faran Shimi Pharmaceutical
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
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ABOUT THIS PAGE
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PharmaCompass offers a list of Estradiol Benzoate 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 Estradiol Benzoate manufacturer or Estradiol Benzoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Estradiol Benzoate manufacturer or Estradiol Benzoate supplier.
PharmaCompass also assists you with knowing the Estradiol Benzoate API Price utilized in the formulation of products. Estradiol Benzoate API Price is not always fixed or binding as the Estradiol Benzoate Price is obtained through a variety of data sources. The Estradiol Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mesalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mesalin, including repackagers and relabelers. The FDA regulates Mesalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mesalin 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 Mesalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mesalin supplier is an individual or a company that provides Mesalin active pharmaceutical ingredient (API) or Mesalin finished formulations upon request. The Mesalin suppliers may include Mesalin API manufacturers, exporters, distributors and traders.
click here to find a list of Mesalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Mesalin DMF (Drug Master File) is a document detailing the whole manufacturing process of Mesalin active pharmaceutical ingredient (API) in detail. Different forms of Mesalin DMFs exist exist since differing nations have different regulations, such as Mesalin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Mesalin DMF submitted to regulatory agencies in the US is known as a USDMF. Mesalin USDMF includes data on Mesalin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Mesalin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Mesalin suppliers with USDMF 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 Mesalin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mesalin 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 Mesalin 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 Mesalin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mesalin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mesalin suppliers with NDC on PharmaCompass.
Mesalin 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 Mesalin 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 Mesalin GMP manufacturer or Mesalin GMP API supplier for your needs.
A Mesalin CoA (Certificate of Analysis) is a formal document that attests to Mesalin's compliance with Mesalin specifications and serves as a tool for batch-level quality control.
Mesalin CoA mostly includes findings from lab analyses of a specific batch. For each Mesalin 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.
Mesalin may be tested according to a variety of international standards, such as European Pharmacopoeia (Mesalin EP), Mesalin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mesalin USP).
