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