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Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
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USDMF
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : Complete
Rev. Date : 2023-08-03
Pay. Date : 2023-07-27
DMF Number : 36959
Submission : 2022-06-16
Status :
Type : II
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PharmaCompass offers a list of Chromic Chloride 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 Chromic Chloride manufacturer or Chromic Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chromic Chloride manufacturer or Chromic Chloride supplier.
PharmaCompass also assists you with knowing the Chromic Chloride API Price utilized in the formulation of products. Chromic Chloride API Price is not always fixed or binding as the Chromic Chloride Price is obtained through a variety of data sources. The Chromic Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hexaaquachromium(III) chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexaaquachromium(III) chloride, including repackagers and relabelers. The FDA regulates Hexaaquachromium(III) chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexaaquachromium(III) chloride supplier is an individual or a company that provides Hexaaquachromium(III) chloride active pharmaceutical ingredient (API) or Hexaaquachromium(III) chloride finished formulations upon request. The Hexaaquachromium(III) chloride suppliers may include Hexaaquachromium(III) chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Hexaaquachromium(III) chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexaaquachromium(III) chloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Hexaaquachromium(III) chloride active pharmaceutical ingredient (API) in detail. Different forms of Hexaaquachromium(III) chloride DMFs exist exist since differing nations have different regulations, such as Hexaaquachromium(III) chloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hexaaquachromium(III) chloride DMF submitted to regulatory agencies in the US is known as a USDMF. Hexaaquachromium(III) chloride USDMF includes data on Hexaaquachromium(III) chloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hexaaquachromium(III) chloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hexaaquachromium(III) chloride suppliers with USDMF on PharmaCompass.
A Hexaaquachromium(III) chloride written confirmation (Hexaaquachromium(III) chloride WC) is an official document issued by a regulatory agency to a Hexaaquachromium(III) chloride manufacturer, verifying that the manufacturing facility of a Hexaaquachromium(III) chloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hexaaquachromium(III) chloride APIs or Hexaaquachromium(III) chloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Hexaaquachromium(III) chloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hexaaquachromium(III) chloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hexaaquachromium(III) chloride suppliers with NDC on PharmaCompass.
Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride 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 Hexaaquachromium(III) chloride GMP manufacturer or Hexaaquachromium(III) chloride GMP API supplier for your needs.
A Hexaaquachromium(III) chloride CoA (Certificate of Analysis) is a formal document that attests to Hexaaquachromium(III) chloride's compliance with Hexaaquachromium(III) chloride specifications and serves as a tool for batch-level quality control.
Hexaaquachromium(III) chloride CoA mostly includes findings from lab analyses of a specific batch. For each Hexaaquachromium(III) chloride 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.
Hexaaquachromium(III) chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Hexaaquachromium(III) chloride EP), Hexaaquachromium(III) chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hexaaquachromium(III) chloride USP).
