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PharmaCompass offers a list of Probucol 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 Probucol manufacturer or Probucol supplier for your needs.
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A MolPort-002-042-265 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-002-042-265, including repackagers and relabelers. The FDA regulates MolPort-002-042-265 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-002-042-265 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A MolPort-002-042-265 supplier is an individual or a company that provides MolPort-002-042-265 active pharmaceutical ingredient (API) or MolPort-002-042-265 finished formulations upon request. The MolPort-002-042-265 suppliers may include MolPort-002-042-265 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-002-042-265 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-002-042-265 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-002-042-265 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-002-042-265 DMFs exist exist since differing nations have different regulations, such as MolPort-002-042-265 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-002-042-265 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-002-042-265 USDMF includes data on MolPort-002-042-265's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-002-042-265 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 MolPort-002-042-265 Drug Master File in Japan (MolPort-002-042-265 JDMF) empowers MolPort-002-042-265 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 MolPort-002-042-265 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-002-042-265 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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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 MolPort-002-042-265 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MolPort-002-042-265 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 MolPort-002-042-265 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 MolPort-002-042-265 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MolPort-002-042-265 NDC to their finished compounded human drug products, they may choose to do so.
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MolPort-002-042-265 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 MolPort-002-042-265 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 MolPort-002-042-265 GMP manufacturer or MolPort-002-042-265 GMP API supplier for your needs.
A MolPort-002-042-265 CoA (Certificate of Analysis) is a formal document that attests to MolPort-002-042-265's compliance with MolPort-002-042-265 specifications and serves as a tool for batch-level quality control.
MolPort-002-042-265 CoA mostly includes findings from lab analyses of a specific batch. For each MolPort-002-042-265 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.
MolPort-002-042-265 may be tested according to a variety of international standards, such as European Pharmacopoeia (MolPort-002-042-265 EP), MolPort-002-042-265 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MolPort-002-042-265 USP).
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