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