API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
0
USA (Orange Book)
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
0
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
36
PharmaCompass offers a list of Benzothiazide 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 Benzothiazide manufacturer or Benzothiazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzothiazide manufacturer or Benzothiazide supplier.
PharmaCompass also assists you with knowing the Benzothiazide API Price utilized in the formulation of products. Benzothiazide API Price is not always fixed or binding as the Benzothiazide Price is obtained through a variety of data sources. The Benzothiazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A benzthiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of benzthiazide, including repackagers and relabelers. The FDA regulates benzthiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. benzthiazide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A benzthiazide supplier is an individual or a company that provides benzthiazide active pharmaceutical ingredient (API) or benzthiazide finished formulations upon request. The benzthiazide suppliers may include benzthiazide API manufacturers, exporters, distributors and traders.
click here to find a list of benzthiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A benzthiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of benzthiazide active pharmaceutical ingredient (API) in detail. Different forms of benzthiazide DMFs exist exist since differing nations have different regulations, such as benzthiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A benzthiazide DMF submitted to regulatory agencies in the US is known as a USDMF. benzthiazide USDMF includes data on benzthiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The benzthiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of benzthiazide suppliers with USDMF on PharmaCompass.
benzthiazide 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 benzthiazide 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 benzthiazide GMP manufacturer or benzthiazide GMP API supplier for your needs.
A benzthiazide CoA (Certificate of Analysis) is a formal document that attests to benzthiazide's compliance with benzthiazide specifications and serves as a tool for batch-level quality control.
benzthiazide CoA mostly includes findings from lab analyses of a specific batch. For each benzthiazide 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.
benzthiazide may be tested according to a variety of international standards, such as European Pharmacopoeia (benzthiazide EP), benzthiazide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (benzthiazide USP).