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ABOUT THIS PAGE
A Chlorothiazide Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorothiazide Sodium, including repackagers and relabelers. The FDA regulates Chlorothiazide Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorothiazide Sodium 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 Chlorothiazide Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorothiazide Sodium supplier is an individual or a company that provides Chlorothiazide Sodium active pharmaceutical ingredient (API) or Chlorothiazide Sodium finished formulations upon request. The Chlorothiazide Sodium suppliers may include Chlorothiazide Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorothiazide Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorothiazide Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Chlorothiazide Sodium active pharmaceutical ingredient (API) in detail. Different forms of Chlorothiazide Sodium DMFs exist exist since differing nations have different regulations, such as Chlorothiazide Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chlorothiazide Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Chlorothiazide Sodium USDMF includes data on Chlorothiazide Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chlorothiazide Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chlorothiazide Sodium suppliers with USDMF on PharmaCompass.
Chlorothiazide Sodium 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 Chlorothiazide Sodium 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 Chlorothiazide Sodium GMP manufacturer or Chlorothiazide Sodium GMP API supplier for your needs.
A Chlorothiazide Sodium CoA (Certificate of Analysis) is a formal document that attests to Chlorothiazide Sodium's compliance with Chlorothiazide Sodium specifications and serves as a tool for batch-level quality control.
Chlorothiazide Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Chlorothiazide Sodium 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.
Chlorothiazide Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Chlorothiazide Sodium EP), Chlorothiazide Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Chlorothiazide Sodium USP).
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