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API SUPPLIERS
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Drugs in Development
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Evonik
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Tiopronin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiopronin, including repackagers and relabelers. The FDA regulates Tiopronin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiopronin 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 Tiopronin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiopronin supplier is an individual or a company that provides Tiopronin active pharmaceutical ingredient (API) or Tiopronin finished formulations upon request. The Tiopronin suppliers may include Tiopronin API manufacturers, exporters, distributors and traders.
click here to find a list of Tiopronin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tiopronin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tiopronin active pharmaceutical ingredient (API) in detail. Different forms of Tiopronin DMFs exist exist since differing nations have different regulations, such as Tiopronin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tiopronin DMF submitted to regulatory agencies in the US is known as a USDMF. Tiopronin USDMF includes data on Tiopronin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tiopronin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tiopronin suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Tiopronin Drug Master File in Japan (Tiopronin JDMF) empowers Tiopronin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Tiopronin JDMF during the approval evaluation for pharmaceutical products. At the time of Tiopronin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Tiopronin suppliers with JDMF on PharmaCompass.
A Tiopronin written confirmation (Tiopronin WC) is an official document issued by a regulatory agency to a Tiopronin manufacturer, verifying that the manufacturing facility of a Tiopronin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tiopronin APIs or Tiopronin finished pharmaceutical products to another nation, regulatory agencies frequently require a Tiopronin WC (written confirmation) as part of the regulatory process.
click here to find a list of Tiopronin 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 Tiopronin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiopronin 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 Tiopronin 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 Tiopronin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiopronin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tiopronin suppliers with NDC on PharmaCompass.
Tiopronin 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 Tiopronin 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 Tiopronin GMP manufacturer or Tiopronin GMP API supplier for your needs.
A Tiopronin CoA (Certificate of Analysis) is a formal document that attests to Tiopronin's compliance with Tiopronin specifications and serves as a tool for batch-level quality control.
Tiopronin CoA mostly includes findings from lab analyses of a specific batch. For each Tiopronin 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.
Tiopronin may be tested according to a variety of international standards, such as European Pharmacopoeia (Tiopronin EP), Tiopronin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tiopronin USP).
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