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