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PharmaCompass offers a list of GET-73 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 GET-73 manufacturer or GET-73 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred GET-73 manufacturer or GET-73 supplier.
PharmaCompass also assists you with knowing the GET-73 API Price utilized in the formulation of products. GET-73 API Price is not always fixed or binding as the GET-73 Price is obtained through a variety of data sources. The GET-73 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GET 73 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GET 73, including repackagers and relabelers. The FDA regulates GET 73 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GET 73 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A GET 73 supplier is an individual or a company that provides GET 73 active pharmaceutical ingredient (API) or GET 73 finished formulations upon request. The GET 73 suppliers may include GET 73 API manufacturers, exporters, distributors and traders.
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 GET 73 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for GET 73 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 GET 73 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 GET 73 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a GET 73 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of GET 73 suppliers with NDC on PharmaCompass.
GET 73 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 GET 73 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 GET 73 GMP manufacturer or GET 73 GMP API supplier for your needs.
A GET 73 CoA (Certificate of Analysis) is a formal document that attests to GET 73's compliance with GET 73 specifications and serves as a tool for batch-level quality control.
GET 73 CoA mostly includes findings from lab analyses of a specific batch. For each GET 73 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.
GET 73 may be tested according to a variety of international standards, such as European Pharmacopoeia (GET 73 EP), GET 73 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (GET 73 USP).
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