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API SUPPLIERS
M2i Group, an integrated CDMO, is your French partner for development & manufacturing in fine chemistry.
TAPI offers customized CDMO Solutions for API development and manufacturing services.
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USDMF
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M2i Group, an integrated CDMO, is your French partner for development & manufacturing in fine chemistry.
About the Company : Integrated solutions for all your projects.
M2i Group provides integrated solutions for all your projects. We offer our clients an integrated partner, from early development...
TAPI offers customized CDMO Solutions for API development and manufacturing services.
About the Company : Founded in 1935, TAPI Technology & API Services has a long-standing tradition of advancing health through innovation and dedication. Today, we proudly build upon this legacy, drivi...
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API Imports and Exports
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INTERMEDIATES SUPPLIERS
Jinan Tantu Chemicals offers customized R&D services & production of small molecule APIs & pharmaceutical intermediates.
CAS Number : 39546-32-2
End Use API : Metopimazine
About The Company : Jinan Tantu Chemicals Co., Ltd. operates as a Contract Development and Manufacturing Organization (CDMO) that serves pharmaceutical companies worldwide. Our cor...
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Metopimazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metopimazine, including repackagers and relabelers. The FDA regulates Metopimazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metopimazine 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 Metopimazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metopimazine supplier is an individual or a company that provides Metopimazine active pharmaceutical ingredient (API) or Metopimazine finished formulations upon request. The Metopimazine suppliers may include Metopimazine API manufacturers, exporters, distributors and traders.
click here to find a list of Metopimazine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Metopimazine DMF (Drug Master File) is a document detailing the whole manufacturing process of Metopimazine active pharmaceutical ingredient (API) in detail. Different forms of Metopimazine DMFs exist exist since differing nations have different regulations, such as Metopimazine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Metopimazine DMF submitted to regulatory agencies in the US is known as a USDMF. Metopimazine USDMF includes data on Metopimazine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Metopimazine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Metopimazine suppliers with USDMF on PharmaCompass.
A Metopimazine written confirmation (Metopimazine WC) is an official document issued by a regulatory agency to a Metopimazine manufacturer, verifying that the manufacturing facility of a Metopimazine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Metopimazine APIs or Metopimazine finished pharmaceutical products to another nation, regulatory agencies frequently require a Metopimazine WC (written confirmation) as part of the regulatory process.
click here to find a list of Metopimazine 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 Metopimazine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Metopimazine 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 Metopimazine 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 Metopimazine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Metopimazine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Metopimazine suppliers with NDC on PharmaCompass.
Metopimazine 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 Metopimazine 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 Metopimazine GMP manufacturer or Metopimazine GMP API supplier for your needs.
A Metopimazine CoA (Certificate of Analysis) is a formal document that attests to Metopimazine's compliance with Metopimazine specifications and serves as a tool for batch-level quality control.
Metopimazine CoA mostly includes findings from lab analyses of a specific batch. For each Metopimazine 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.
Metopimazine may be tested according to a variety of international standards, such as European Pharmacopoeia (Metopimazine EP), Metopimazine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Metopimazine USP).
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