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PharmaCompass offers a list of Sodium Allopurinol 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 Sodium Allopurinol manufacturer or Sodium Allopurinol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Allopurinol manufacturer or Sodium Allopurinol supplier.
PharmaCompass also assists you with knowing the Sodium Allopurinol API Price utilized in the formulation of products. Sodium Allopurinol API Price is not always fixed or binding as the Sodium Allopurinol Price is obtained through a variety of data sources. The Sodium Allopurinol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium Allopurinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Allopurinol, including repackagers and relabelers. The FDA regulates Sodium Allopurinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Allopurinol 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 Sodium Allopurinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Allopurinol supplier is an individual or a company that provides Sodium Allopurinol active pharmaceutical ingredient (API) or Sodium Allopurinol finished formulations upon request. The Sodium Allopurinol suppliers may include Sodium Allopurinol API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Allopurinol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Sodium Allopurinol 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 Sodium Allopurinol 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 Sodium Allopurinol GMP manufacturer or Sodium Allopurinol GMP API supplier for your needs.
A Sodium Allopurinol CoA (Certificate of Analysis) is a formal document that attests to Sodium Allopurinol's compliance with Sodium Allopurinol specifications and serves as a tool for batch-level quality control.
Sodium Allopurinol CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Allopurinol 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.
Sodium Allopurinol may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Allopurinol EP), Sodium Allopurinol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Allopurinol USP).
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