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PharmaCompass offers a list of Isoproterenol 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 Isoproterenol manufacturer or Isoproterenol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isoproterenol manufacturer or Isoproterenol supplier.
PharmaCompass also assists you with knowing the Isoproterenol API Price utilized in the formulation of products. Isoproterenol API Price is not always fixed or binding as the Isoproterenol Price is obtained through a variety of data sources. The Isoproterenol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Isuprel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isuprel, including repackagers and relabelers. The FDA regulates Isuprel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isuprel 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 Isuprel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Isuprel supplier is an individual or a company that provides Isuprel active pharmaceutical ingredient (API) or Isuprel finished formulations upon request. The Isuprel suppliers may include Isuprel API manufacturers, exporters, distributors and traders.
click here to find a list of Isuprel suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Isuprel DMF (Drug Master File) is a document detailing the whole manufacturing process of Isuprel active pharmaceutical ingredient (API) in detail. Different forms of Isuprel DMFs exist exist since differing nations have different regulations, such as Isuprel USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Isuprel DMF submitted to regulatory agencies in the US is known as a USDMF. Isuprel USDMF includes data on Isuprel's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Isuprel USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Isuprel suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Isuprel Drug Master File in Japan (Isuprel JDMF) empowers Isuprel API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Isuprel JDMF during the approval evaluation for pharmaceutical products. At the time of Isuprel JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Isuprel suppliers with JDMF on PharmaCompass.
A Isuprel CEP of the European Pharmacopoeia monograph is often referred to as a Isuprel Certificate of Suitability (COS). The purpose of a Isuprel CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Isuprel EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Isuprel to their clients by showing that a Isuprel CEP has been issued for it. The manufacturer submits a Isuprel CEP (COS) as part of the market authorization procedure, and it takes on the role of a Isuprel CEP holder for the record. Additionally, the data presented in the Isuprel CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Isuprel DMF.
A Isuprel CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Isuprel CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Isuprel suppliers with CEP (COS) on PharmaCompass.
A Isuprel written confirmation (Isuprel WC) is an official document issued by a regulatory agency to a Isuprel manufacturer, verifying that the manufacturing facility of a Isuprel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Isuprel APIs or Isuprel finished pharmaceutical products to another nation, regulatory agencies frequently require a Isuprel WC (written confirmation) as part of the regulatory process.
click here to find a list of Isuprel 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 Isuprel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Isuprel 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 Isuprel 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 Isuprel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Isuprel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Isuprel suppliers with NDC on PharmaCompass.
Isuprel 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 Isuprel 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 Isuprel GMP manufacturer or Isuprel GMP API supplier for your needs.
A Isuprel CoA (Certificate of Analysis) is a formal document that attests to Isuprel's compliance with Isuprel specifications and serves as a tool for batch-level quality control.
Isuprel CoA mostly includes findings from lab analyses of a specific batch. For each Isuprel 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.
Isuprel may be tested according to a variety of international standards, such as European Pharmacopoeia (Isuprel EP), Isuprel JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Isuprel USP).