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