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PharmaCompass offers a list of Hydrochlorothiazide 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 Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier.
PharmaCompass also assists you with knowing the Hydrochlorothiazide API Price utilized in the formulation of products. Hydrochlorothiazide API Price is not always fixed or binding as the Hydrochlorothiazide Price is obtained through a variety of data sources. The Hydrochlorothiazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydrochlorothiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrochlorothiazide, including repackagers and relabelers. The FDA regulates Hydrochlorothiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrochlorothiazide 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 Hydrochlorothiazide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrochlorothiazide supplier is an individual or a company that provides Hydrochlorothiazide active pharmaceutical ingredient (API) or Hydrochlorothiazide finished formulations upon request. The Hydrochlorothiazide suppliers may include Hydrochlorothiazide API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrochlorothiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hydrochlorothiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of Hydrochlorothiazide active pharmaceutical ingredient (API) in detail. Different forms of Hydrochlorothiazide DMFs exist exist since differing nations have different regulations, such as Hydrochlorothiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hydrochlorothiazide DMF submitted to regulatory agencies in the US is known as a USDMF. Hydrochlorothiazide USDMF includes data on Hydrochlorothiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hydrochlorothiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hydrochlorothiazide suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Hydrochlorothiazide Drug Master File in Japan (Hydrochlorothiazide JDMF) empowers Hydrochlorothiazide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Hydrochlorothiazide JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrochlorothiazide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Hydrochlorothiazide suppliers with JDMF 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 Hydrochlorothiazide Drug Master File in Korea (Hydrochlorothiazide KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Hydrochlorothiazide. The MFDS reviews the Hydrochlorothiazide KDMF as part of the drug registration process and uses the information provided in the Hydrochlorothiazide KDMF to evaluate the safety and efficacy of the drug.
After submitting a Hydrochlorothiazide 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 Hydrochlorothiazide API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Hydrochlorothiazide suppliers with KDMF on PharmaCompass.
A Hydrochlorothiazide CEP of the European Pharmacopoeia monograph is often referred to as a Hydrochlorothiazide Certificate of Suitability (COS). The purpose of a Hydrochlorothiazide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydrochlorothiazide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydrochlorothiazide to their clients by showing that a Hydrochlorothiazide CEP has been issued for it. The manufacturer submits a Hydrochlorothiazide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydrochlorothiazide CEP holder for the record. Additionally, the data presented in the Hydrochlorothiazide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydrochlorothiazide DMF.
A Hydrochlorothiazide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydrochlorothiazide 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 Hydrochlorothiazide suppliers with CEP (COS) on PharmaCompass.
A Hydrochlorothiazide written confirmation (Hydrochlorothiazide WC) is an official document issued by a regulatory agency to a Hydrochlorothiazide manufacturer, verifying that the manufacturing facility of a Hydrochlorothiazide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Hydrochlorothiazide APIs or Hydrochlorothiazide finished pharmaceutical products to another nation, regulatory agencies frequently require a Hydrochlorothiazide WC (written confirmation) as part of the regulatory process.
click here to find a list of Hydrochlorothiazide 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 Hydrochlorothiazide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydrochlorothiazide 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 Hydrochlorothiazide 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 Hydrochlorothiazide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydrochlorothiazide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydrochlorothiazide suppliers with NDC on PharmaCompass.
Hydrochlorothiazide 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 Hydrochlorothiazide 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 Hydrochlorothiazide GMP manufacturer or Hydrochlorothiazide GMP API supplier for your needs.
A Hydrochlorothiazide CoA (Certificate of Analysis) is a formal document that attests to Hydrochlorothiazide's compliance with Hydrochlorothiazide specifications and serves as a tool for batch-level quality control.
Hydrochlorothiazide CoA mostly includes findings from lab analyses of a specific batch. For each Hydrochlorothiazide 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.
Hydrochlorothiazide may be tested according to a variety of international standards, such as European Pharmacopoeia (Hydrochlorothiazide EP), Hydrochlorothiazide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Hydrochlorothiazide USP).
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