Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
VMF
0
Listed Suppliers
0
Europe
0
Canada
0
Australia
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]NDC API
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Digital Content
NEWS #PharmaBuzz
Market Place
ABOUT THIS PAGE
A Copper Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Copper Chloride, including repackagers and relabelers. The FDA regulates Copper Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Copper 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.
A Copper Chloride supplier is an individual or a company that provides Copper Chloride active pharmaceutical ingredient (API) or Copper Chloride finished formulations upon request. The Copper Chloride suppliers may include Copper Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Copper Chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Copper Chloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Copper Chloride active pharmaceutical ingredient (API) in detail. Different forms of Copper Chloride DMFs exist exist since differing nations have different regulations, such as Copper Chloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Copper Chloride DMF submitted to regulatory agencies in the US is known as a USDMF. Copper Chloride USDMF includes data on Copper Chloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Copper Chloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Copper Chloride 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 Copper Chloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Copper 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 Copper 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 Copper Chloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Copper Chloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Copper Chloride suppliers with NDC on PharmaCompass.
Copper 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 Copper 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 Copper Chloride GMP manufacturer or Copper Chloride GMP API supplier for your needs.
A Copper Chloride CoA (Certificate of Analysis) is a formal document that attests to Copper Chloride's compliance with Copper Chloride specifications and serves as a tool for batch-level quality control.
Copper Chloride CoA mostly includes findings from lab analyses of a specific batch. For each Copper 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.
Copper Chloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Copper Chloride EP), Copper Chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Copper Chloride USP).
LOOKING FOR A SUPPLIER?
