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PharmaCompass offers a list of Green Tea Extract 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 Green Tea Extract manufacturer or Green Tea Extract supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Green Tea Extract manufacturer or Green Tea Extract supplier.
PharmaCompass also assists you with knowing the Green Tea Extract API Price utilized in the formulation of products. Green Tea Extract API Price is not always fixed or binding as the Green Tea Extract Price is obtained through a variety of data sources. The Green Tea Extract Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Green Tea manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Green Tea, including repackagers and relabelers. The FDA regulates Green Tea manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Green Tea 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 Green Tea manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Green Tea supplier is an individual or a company that provides Green Tea active pharmaceutical ingredient (API) or Green Tea finished formulations upon request. The Green Tea suppliers may include Green Tea API manufacturers, exporters, distributors and traders.
click here to find a list of Green Tea suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Green Tea DMF (Drug Master File) is a document detailing the whole manufacturing process of Green Tea active pharmaceutical ingredient (API) in detail. Different forms of Green Tea DMFs exist exist since differing nations have different regulations, such as Green Tea USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Green Tea DMF submitted to regulatory agencies in the US is known as a USDMF. Green Tea USDMF includes data on Green Tea's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Green Tea USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Green Tea suppliers with USDMF 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 Green Tea as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Green Tea 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 Green Tea 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 Green Tea and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Green Tea NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Green Tea suppliers with NDC on PharmaCompass.
Green Tea 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 Green Tea 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 Green Tea GMP manufacturer or Green Tea GMP API supplier for your needs.
A Green Tea CoA (Certificate of Analysis) is a formal document that attests to Green Tea's compliance with Green Tea specifications and serves as a tool for batch-level quality control.
Green Tea CoA mostly includes findings from lab analyses of a specific batch. For each Green Tea 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.
Green Tea may be tested according to a variety of international standards, such as European Pharmacopoeia (Green Tea EP), Green Tea JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Green Tea USP).
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