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PharmaCompass offers a list of Meglumine Antimonate 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 Meglumine Antimonate manufacturer or Meglumine Antimonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Meglumine Antimonate manufacturer or Meglumine Antimonate supplier.
PharmaCompass also assists you with knowing the Meglumine Antimonate API Price utilized in the formulation of products. Meglumine Antimonate API Price is not always fixed or binding as the Meglumine Antimonate Price is obtained through a variety of data sources. The Meglumine Antimonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Meglumine Antimonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Meglumine Antimonate, including repackagers and relabelers. The FDA regulates Meglumine Antimonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Meglumine Antimonate 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 Meglumine Antimonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Meglumine Antimonate supplier is an individual or a company that provides Meglumine Antimonate active pharmaceutical ingredient (API) or Meglumine Antimonate finished formulations upon request. The Meglumine Antimonate suppliers may include Meglumine Antimonate API manufacturers, exporters, distributors and traders.
click here to find a list of Meglumine Antimonate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Meglumine Antimonate DMF (Drug Master File) is a document detailing the whole manufacturing process of Meglumine Antimonate active pharmaceutical ingredient (API) in detail. Different forms of Meglumine Antimonate DMFs exist exist since differing nations have different regulations, such as Meglumine Antimonate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Meglumine Antimonate DMF submitted to regulatory agencies in the US is known as a USDMF. Meglumine Antimonate USDMF includes data on Meglumine Antimonate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Meglumine Antimonate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Meglumine Antimonate suppliers with USDMF on PharmaCompass.
Meglumine Antimonate 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 Meglumine Antimonate 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 Meglumine Antimonate GMP manufacturer or Meglumine Antimonate GMP API supplier for your needs.
A Meglumine Antimonate CoA (Certificate of Analysis) is a formal document that attests to Meglumine Antimonate's compliance with Meglumine Antimonate specifications and serves as a tool for batch-level quality control.
Meglumine Antimonate CoA mostly includes findings from lab analyses of a specific batch. For each Meglumine Antimonate 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.
Meglumine Antimonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Meglumine Antimonate EP), Meglumine Antimonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Meglumine Antimonate USP).
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