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