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NDC API
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Stock Recap #PipelineProspector
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DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 43%
USFDA APPLICATION NUMBER - 13295
DOSAGE - INJECTABLE;INJECTION - 60%
USFDA APPLICATION NUMBER - 13295
DOSAGE - INJECTABLE;INJECTION - 30%
USFDA APPLICATION NUMBER - 16983
Digital Content
DATA COMPILATION #PharmaFlow
ABOUT THIS PAGE
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PharmaCompass offers a list of Iothalamate Meglumine 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 Iothalamate Meglumine manufacturer or Iothalamate Meglumine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iothalamate Meglumine manufacturer or Iothalamate Meglumine supplier.
PharmaCompass also assists you with knowing the Iothalamate Meglumine API Price utilized in the formulation of products. Iothalamate Meglumine API Price is not always fixed or binding as the Iothalamate Meglumine Price is obtained through a variety of data sources. The Iothalamate Meglumine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Conray 280 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Conray 280, including repackagers and relabelers. The FDA regulates Conray 280 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Conray 280 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Conray 280 supplier is an individual or a company that provides Conray 280 active pharmaceutical ingredient (API) or Conray 280 finished formulations upon request. The Conray 280 suppliers may include Conray 280 API manufacturers, exporters, distributors and traders.
Conray 280 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 Conray 280 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 Conray 280 GMP manufacturer or Conray 280 GMP API supplier for your needs.
A Conray 280 CoA (Certificate of Analysis) is a formal document that attests to Conray 280's compliance with Conray 280 specifications and serves as a tool for batch-level quality control.
Conray 280 CoA mostly includes findings from lab analyses of a specific batch. For each Conray 280 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.
Conray 280 may be tested according to a variety of international standards, such as European Pharmacopoeia (Conray 280 EP), Conray 280 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Conray 280 USP).
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