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PharmaCompass offers a list of 7-Ethyl-10-Hydroxycamptothecin 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 7-Ethyl-10-Hydroxycamptothecin manufacturer or 7-Ethyl-10-Hydroxycamptothecin supplier for your needs.
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PharmaCompass also assists you with knowing the 7-Ethyl-10-Hydroxycamptothecin API Price utilized in the formulation of products. 7-Ethyl-10-Hydroxycamptothecin API Price is not always fixed or binding as the 7-Ethyl-10-Hydroxycamptothecin Price is obtained through a variety of data sources. The 7-Ethyl-10-Hydroxycamptothecin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SN38 API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SN38 API, including repackagers and relabelers. The FDA regulates SN38 API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SN38 API 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 SN38 API manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SN38 API supplier is an individual or a company that provides SN38 API active pharmaceutical ingredient (API) or SN38 API finished formulations upon request. The SN38 API suppliers may include SN38 API API manufacturers, exporters, distributors and traders.
click here to find a list of SN38 API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 SN38 API as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for SN38 API 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 SN38 API 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 SN38 API and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a SN38 API NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of SN38 API suppliers with NDC on PharmaCompass.
SN38 API 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 SN38 API 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 SN38 API GMP manufacturer or SN38 API GMP API supplier for your needs.
A SN38 API CoA (Certificate of Analysis) is a formal document that attests to SN38 API's compliance with SN38 API specifications and serves as a tool for batch-level quality control.
SN38 API CoA mostly includes findings from lab analyses of a specific batch. For each SN38 API 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.
SN38 API may be tested according to a variety of international standards, such as European Pharmacopoeia (SN38 API EP), SN38 API JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SN38 API USP).