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PharmaCompass offers a list of Hydroquinone 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 Hydroquinone manufacturer or Hydroquinone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroquinone manufacturer or Hydroquinone supplier.
PharmaCompass also assists you with knowing the Hydroquinone API Price utilized in the formulation of products. Hydroquinone API Price is not always fixed or binding as the Hydroquinone Price is obtained through a variety of data sources. The Hydroquinone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 094CADDB-59BF-4EDF-B278-59791B203EA2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 094CADDB-59BF-4EDF-B278-59791B203EA2, including repackagers and relabelers. The FDA regulates 094CADDB-59BF-4EDF-B278-59791B203EA2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 094CADDB-59BF-4EDF-B278-59791B203EA2 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 094CADDB-59BF-4EDF-B278-59791B203EA2 supplier is an individual or a company that provides 094CADDB-59BF-4EDF-B278-59791B203EA2 active pharmaceutical ingredient (API) or 094CADDB-59BF-4EDF-B278-59791B203EA2 finished formulations upon request. The 094CADDB-59BF-4EDF-B278-59791B203EA2 suppliers may include 094CADDB-59BF-4EDF-B278-59791B203EA2 API manufacturers, exporters, distributors and traders.
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A 094CADDB-59BF-4EDF-B278-59791B203EA2 DMF (Drug Master File) is a document detailing the whole manufacturing process of 094CADDB-59BF-4EDF-B278-59791B203EA2 active pharmaceutical ingredient (API) in detail. Different forms of 094CADDB-59BF-4EDF-B278-59791B203EA2 DMFs exist exist since differing nations have different regulations, such as 094CADDB-59BF-4EDF-B278-59791B203EA2 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 094CADDB-59BF-4EDF-B278-59791B203EA2 DMF submitted to regulatory agencies in the US is known as a USDMF. 094CADDB-59BF-4EDF-B278-59791B203EA2 USDMF includes data on 094CADDB-59BF-4EDF-B278-59791B203EA2's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 094CADDB-59BF-4EDF-B278-59791B203EA2 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A 094CADDB-59BF-4EDF-B278-59791B203EA2 written confirmation (094CADDB-59BF-4EDF-B278-59791B203EA2 WC) is an official document issued by a regulatory agency to a 094CADDB-59BF-4EDF-B278-59791B203EA2 manufacturer, verifying that the manufacturing facility of a 094CADDB-59BF-4EDF-B278-59791B203EA2 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 094CADDB-59BF-4EDF-B278-59791B203EA2 APIs or 094CADDB-59BF-4EDF-B278-59791B203EA2 finished pharmaceutical products to another nation, regulatory agencies frequently require a 094CADDB-59BF-4EDF-B278-59791B203EA2 WC (written confirmation) as part of the regulatory process.
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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 094CADDB-59BF-4EDF-B278-59791B203EA2 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 094CADDB-59BF-4EDF-B278-59791B203EA2 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 094CADDB-59BF-4EDF-B278-59791B203EA2 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 094CADDB-59BF-4EDF-B278-59791B203EA2 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 094CADDB-59BF-4EDF-B278-59791B203EA2 NDC to their finished compounded human drug products, they may choose to do so.
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094CADDB-59BF-4EDF-B278-59791B203EA2 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 094CADDB-59BF-4EDF-B278-59791B203EA2 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 094CADDB-59BF-4EDF-B278-59791B203EA2 GMP manufacturer or 094CADDB-59BF-4EDF-B278-59791B203EA2 GMP API supplier for your needs.
A 094CADDB-59BF-4EDF-B278-59791B203EA2 CoA (Certificate of Analysis) is a formal document that attests to 094CADDB-59BF-4EDF-B278-59791B203EA2's compliance with 094CADDB-59BF-4EDF-B278-59791B203EA2 specifications and serves as a tool for batch-level quality control.
094CADDB-59BF-4EDF-B278-59791B203EA2 CoA mostly includes findings from lab analyses of a specific batch. For each 094CADDB-59BF-4EDF-B278-59791B203EA2 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.
094CADDB-59BF-4EDF-B278-59791B203EA2 may be tested according to a variety of international standards, such as European Pharmacopoeia (094CADDB-59BF-4EDF-B278-59791B203EA2 EP), 094CADDB-59BF-4EDF-B278-59791B203EA2 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (094CADDB-59BF-4EDF-B278-59791B203EA2 USP).
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