X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
21
PharmaCompass offers a list of Benazepril 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 Benazepril manufacturer or Benazepril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benazepril manufacturer or Benazepril supplier.
PharmaCompass also assists you with knowing the Benazepril API Price utilized in the formulation of products. Benazepril API Price is not always fixed or binding as the Benazepril Price is obtained through a variety of data sources. The Benazepril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Benazeprilat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benazeprilat, including repackagers and relabelers. The FDA regulates Benazeprilat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benazeprilat 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 Benazeprilat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benazeprilat supplier is an individual or a company that provides Benazeprilat active pharmaceutical ingredient (API) or Benazeprilat finished formulations upon request. The Benazeprilat suppliers may include Benazeprilat API manufacturers, exporters, distributors and traders.
click here to find a list of Benazeprilat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Benazeprilat DMF (Drug Master File) is a document detailing the whole manufacturing process of Benazeprilat active pharmaceutical ingredient (API) in detail. Different forms of Benazeprilat DMFs exist exist since differing nations have different regulations, such as Benazeprilat USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Benazeprilat DMF submitted to regulatory agencies in the US is known as a USDMF. Benazeprilat USDMF includes data on Benazeprilat's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Benazeprilat USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Benazeprilat suppliers with USDMF on PharmaCompass.
Benazeprilat 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 Benazeprilat 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 Benazeprilat GMP manufacturer or Benazeprilat GMP API supplier for your needs.
A Benazeprilat CoA (Certificate of Analysis) is a formal document that attests to Benazeprilat's compliance with Benazeprilat specifications and serves as a tool for batch-level quality control.
Benazeprilat CoA mostly includes findings from lab analyses of a specific batch. For each Benazeprilat 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.
Benazeprilat may be tested according to a variety of international standards, such as European Pharmacopoeia (Benazeprilat EP), Benazeprilat JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Benazeprilat USP).
Market Place
