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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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ABOUT THIS PAGE
43
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 Chromium chloride hexahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chromium chloride hexahydrate, including repackagers and relabelers. The FDA regulates Chromium chloride hexahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chromium chloride hexahydrate 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 Chromium chloride hexahydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chromium chloride hexahydrate supplier is an individual or a company that provides Chromium chloride hexahydrate active pharmaceutical ingredient (API) or Chromium chloride hexahydrate finished formulations upon request. The Chromium chloride hexahydrate suppliers may include Chromium chloride hexahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Chromium chloride hexahydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chromium chloride hexahydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Chromium chloride hexahydrate active pharmaceutical ingredient (API) in detail. Different forms of Chromium chloride hexahydrate DMFs exist exist since differing nations have different regulations, such as Chromium chloride hexahydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chromium chloride hexahydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Chromium chloride hexahydrate USDMF includes data on Chromium chloride hexahydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chromium chloride hexahydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chromium chloride hexahydrate suppliers with USDMF 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 Chromium chloride hexahydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Chromium chloride hexahydrate 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 Chromium chloride hexahydrate 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 Chromium chloride hexahydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Chromium chloride hexahydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Chromium chloride hexahydrate suppliers with NDC on PharmaCompass.
Chromium chloride hexahydrate 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 Chromium chloride hexahydrate 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 Chromium chloride hexahydrate GMP manufacturer or Chromium chloride hexahydrate GMP API supplier for your needs.
A Chromium chloride hexahydrate CoA (Certificate of Analysis) is a formal document that attests to Chromium chloride hexahydrate's compliance with Chromium chloride hexahydrate specifications and serves as a tool for batch-level quality control.
Chromium chloride hexahydrate CoA mostly includes findings from lab analyses of a specific batch. For each Chromium chloride hexahydrate 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.
Chromium chloride hexahydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Chromium chloride hexahydrate EP), Chromium chloride hexahydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chromium chloride hexahydrate USP).
