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DOSAGE - SOLUTION;INTRAVENOUS - EQ 10MG BASE/...DOSAGE - SOLUTION;INTRAVENOUS - EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
USFDA APPLICATION NUMBER - 20098
DOSAGE - SOLUTION;INTRAVENOUS - EQ 20MG BASE/...DOSAGE - SOLUTION;INTRAVENOUS - EQ 20MG BASE/10ML (EQ 2MG BASE/ML)
USFDA APPLICATION NUMBER - 20098
DOSAGE - SOLUTION;INTRAVENOUS - EQ 2MG BASE/M...DOSAGE - SOLUTION;INTRAVENOUS - EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 20098
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PharmaCompass offers a list of Mivacurium 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 Mivacurium Chloride manufacturer or Mivacurium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mivacurium Chloride manufacturer or Mivacurium Chloride supplier.
PharmaCompass also assists you with knowing the Mivacurium Chloride API Price utilized in the formulation of products. Mivacurium Chloride API Price is not always fixed or binding as the Mivacurium Chloride Price is obtained through a variety of data sources. The Mivacurium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cloruro de mivacurio manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloruro de mivacurio, including repackagers and relabelers. The FDA regulates Cloruro de mivacurio manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloruro de mivacurio 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 Cloruro de mivacurio manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cloruro de mivacurio supplier is an individual or a company that provides Cloruro de mivacurio active pharmaceutical ingredient (API) or Cloruro de mivacurio finished formulations upon request. The Cloruro de mivacurio suppliers may include Cloruro de mivacurio API manufacturers, exporters, distributors and traders.
click here to find a list of Cloruro de mivacurio suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cloruro de mivacurio DMF (Drug Master File) is a document detailing the whole manufacturing process of Cloruro de mivacurio active pharmaceutical ingredient (API) in detail. Different forms of Cloruro de mivacurio DMFs exist exist since differing nations have different regulations, such as Cloruro de mivacurio USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cloruro de mivacurio DMF submitted to regulatory agencies in the US is known as a USDMF. Cloruro de mivacurio USDMF includes data on Cloruro de mivacurio's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cloruro de mivacurio USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cloruro de mivacurio 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 Cloruro de mivacurio as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cloruro de mivacurio 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 Cloruro de mivacurio 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 Cloruro de mivacurio and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cloruro de mivacurio NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cloruro de mivacurio suppliers with NDC on PharmaCompass.
Cloruro de mivacurio 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 Cloruro de mivacurio 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 Cloruro de mivacurio GMP manufacturer or Cloruro de mivacurio GMP API supplier for your needs.
A Cloruro de mivacurio CoA (Certificate of Analysis) is a formal document that attests to Cloruro de mivacurio's compliance with Cloruro de mivacurio specifications and serves as a tool for batch-level quality control.
Cloruro de mivacurio CoA mostly includes findings from lab analyses of a specific batch. For each Cloruro de mivacurio 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.
Cloruro de mivacurio may be tested according to a variety of international standards, such as European Pharmacopoeia (Cloruro de mivacurio EP), Cloruro de mivacurio JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cloruro de mivacurio USP).
