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PharmaCompass offers a list of Promethazine 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 Promethazine manufacturer or Promethazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Promethazine manufacturer or Promethazine supplier.
PharmaCompass also assists you with knowing the Promethazine API Price utilized in the formulation of products. Promethazine API Price is not always fixed or binding as the Promethazine Price is obtained through a variety of data sources. The Promethazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Histargan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histargan, including repackagers and relabelers. The FDA regulates Histargan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histargan 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 Histargan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histargan supplier is an individual or a company that provides Histargan active pharmaceutical ingredient (API) or Histargan finished formulations upon request. The Histargan suppliers may include Histargan API manufacturers, exporters, distributors and traders.
click here to find a list of Histargan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Histargan Drug Master File in Japan (Histargan JDMF) empowers Histargan API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Histargan JDMF during the approval evaluation for pharmaceutical products. At the time of Histargan JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Histargan suppliers with JDMF on PharmaCompass.
Histargan 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 Histargan 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 Histargan GMP manufacturer or Histargan GMP API supplier for your needs.
A Histargan CoA (Certificate of Analysis) is a formal document that attests to Histargan's compliance with Histargan specifications and serves as a tool for batch-level quality control.
Histargan CoA mostly includes findings from lab analyses of a specific batch. For each Histargan 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.
Histargan may be tested according to a variety of international standards, such as European Pharmacopoeia (Histargan EP), Histargan JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Histargan USP).
