API Suppliers
US DMFs Filed
0
CEP/COS Certifications
JDMFs Filed
0
EU WC
Listed Suppliers
USA (Orange Book)
0
Europe
Canada
Australia
0
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
78
PharmaCompass offers a list of Flunarizine 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 Flunarizine manufacturer or Flunarizine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flunarizine manufacturer or Flunarizine supplier.
PharmaCompass also assists you with knowing the Flunarizine API Price utilized in the formulation of products. Flunarizine API Price is not always fixed or binding as the Flunarizine Price is obtained through a variety of data sources. The Flunarizine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flunarizine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flunarizine Hydrochloride, including repackagers and relabelers. The FDA regulates Flunarizine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flunarizine Hydrochloride 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 Flunarizine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flunarizine Hydrochloride supplier is an individual or a company that provides Flunarizine Hydrochloride active pharmaceutical ingredient (API) or Flunarizine Hydrochloride finished formulations upon request. The Flunarizine Hydrochloride suppliers may include Flunarizine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Flunarizine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Flunarizine Hydrochloride Drug Master File in Korea (Flunarizine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Flunarizine Hydrochloride. The MFDS reviews the Flunarizine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Flunarizine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Flunarizine Hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Flunarizine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Flunarizine Hydrochloride suppliers with KDMF on PharmaCompass.
A Flunarizine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Flunarizine Hydrochloride Certificate of Suitability (COS). The purpose of a Flunarizine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flunarizine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flunarizine Hydrochloride to their clients by showing that a Flunarizine Hydrochloride CEP has been issued for it. The manufacturer submits a Flunarizine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flunarizine Hydrochloride CEP holder for the record. Additionally, the data presented in the Flunarizine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flunarizine Hydrochloride DMF.
A Flunarizine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flunarizine Hydrochloride 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 Flunarizine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
A Flunarizine Hydrochloride written confirmation (Flunarizine Hydrochloride WC) is an official document issued by a regulatory agency to a Flunarizine Hydrochloride manufacturer, verifying that the manufacturing facility of a Flunarizine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Flunarizine Hydrochloride APIs or Flunarizine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Flunarizine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Flunarizine Hydrochloride 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 Flunarizine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flunarizine Hydrochloride 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 Flunarizine Hydrochloride 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 Flunarizine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flunarizine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Flunarizine Hydrochloride suppliers with NDC on PharmaCompass.
Flunarizine Hydrochloride 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 Flunarizine Hydrochloride 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 Flunarizine Hydrochloride GMP manufacturer or Flunarizine Hydrochloride GMP API supplier for your needs.
A Flunarizine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Flunarizine Hydrochloride's compliance with Flunarizine Hydrochloride specifications and serves as a tool for batch-level quality control.
Flunarizine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Flunarizine Hydrochloride 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.
Flunarizine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Flunarizine Hydrochloride EP), Flunarizine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Flunarizine Hydrochloride USP).