API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
EU WC
Listed Suppliers
0
USA (Orange Book)
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
31
PharmaCompass offers a list of Isosulfan Blue 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 Isosulfan Blue manufacturer or Isosulfan Blue supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isosulfan Blue manufacturer or Isosulfan Blue supplier.
PharmaCompass also assists you with knowing the Isosulfan Blue API Price utilized in the formulation of products. Isosulfan Blue API Price is not always fixed or binding as the Isosulfan Blue Price is obtained through a variety of data sources. The Isosulfan Blue Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Isosulfan Blue manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isosulfan Blue, including repackagers and relabelers. The FDA regulates Isosulfan Blue manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isosulfan Blue 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 Isosulfan Blue manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Isosulfan Blue supplier is an individual or a company that provides Isosulfan Blue active pharmaceutical ingredient (API) or Isosulfan Blue finished formulations upon request. The Isosulfan Blue suppliers may include Isosulfan Blue API manufacturers, exporters, distributors and traders.
click here to find a list of Isosulfan Blue suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Isosulfan Blue DMF (Drug Master File) is a document detailing the whole manufacturing process of Isosulfan Blue active pharmaceutical ingredient (API) in detail. Different forms of Isosulfan Blue DMFs exist exist since differing nations have different regulations, such as Isosulfan Blue USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Isosulfan Blue DMF submitted to regulatory agencies in the US is known as a USDMF. Isosulfan Blue USDMF includes data on Isosulfan Blue's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Isosulfan Blue USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Isosulfan Blue suppliers with USDMF on PharmaCompass.
A Isosulfan Blue written confirmation (Isosulfan Blue WC) is an official document issued by a regulatory agency to a Isosulfan Blue manufacturer, verifying that the manufacturing facility of a Isosulfan Blue active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Isosulfan Blue APIs or Isosulfan Blue finished pharmaceutical products to another nation, regulatory agencies frequently require a Isosulfan Blue WC (written confirmation) as part of the regulatory process.
click here to find a list of Isosulfan Blue 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 Isosulfan Blue as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Isosulfan Blue 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 Isosulfan Blue 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 Isosulfan Blue and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Isosulfan Blue NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Isosulfan Blue suppliers with NDC on PharmaCompass.
Isosulfan Blue 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 Isosulfan Blue 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 Isosulfan Blue GMP manufacturer or Isosulfan Blue GMP API supplier for your needs.
A Isosulfan Blue CoA (Certificate of Analysis) is a formal document that attests to Isosulfan Blue's compliance with Isosulfan Blue specifications and serves as a tool for batch-level quality control.
Isosulfan Blue CoA mostly includes findings from lab analyses of a specific batch. For each Isosulfan Blue 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.
Isosulfan Blue may be tested according to a variety of international standards, such as European Pharmacopoeia (Isosulfan Blue EP), Isosulfan Blue JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Isosulfan Blue USP).