Synopsis
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USDMF
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JP
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API
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API SUPPLIERS
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EU WC
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ABOUT THIS PAGE
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PharmaCompass offers a list of Chlorcyclizine Hydrochloride 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 Chlorcyclizine Hydrochloride manufacturer or Chlorcyclizine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorcyclizine Hydrochloride manufacturer or Chlorcyclizine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Chlorcyclizine Hydrochloride API Price utilized in the formulation of products. Chlorcyclizine Hydrochloride API Price is not always fixed or binding as the Chlorcyclizine Hydrochloride Price is obtained through a variety of data sources. The Chlorcyclizine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Di-Paralene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Di-Paralene, including repackagers and relabelers. The FDA regulates Di-Paralene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Di-Paralene 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 Di-Paralene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Di-Paralene supplier is an individual or a company that provides Di-Paralene active pharmaceutical ingredient (API) or Di-Paralene finished formulations upon request. The Di-Paralene suppliers may include Di-Paralene API manufacturers, exporters, distributors and traders.
click here to find a list of Di-Paralene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Di-Paralene written confirmation (Di-Paralene WC) is an official document issued by a regulatory agency to a Di-Paralene manufacturer, verifying that the manufacturing facility of a Di-Paralene active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Di-Paralene APIs or Di-Paralene finished pharmaceutical products to another nation, regulatory agencies frequently require a Di-Paralene WC (written confirmation) as part of the regulatory process.
click here to find a list of Di-Paralene suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Di-Paralene as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Di-Paralene API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Di-Paralene as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Di-Paralene and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Di-Paralene NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Di-Paralene suppliers with NDC on PharmaCompass.
Di-Paralene 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 Di-Paralene 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 Di-Paralene GMP manufacturer or Di-Paralene GMP API supplier for your needs.
A Di-Paralene CoA (Certificate of Analysis) is a formal document that attests to Di-Paralene's compliance with Di-Paralene specifications and serves as a tool for batch-level quality control.
Di-Paralene CoA mostly includes findings from lab analyses of a specific batch. For each Di-Paralene 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.
Di-Paralene may be tested according to a variety of international standards, such as European Pharmacopoeia (Di-Paralene EP), Di-Paralene JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Di-Paralene USP).
