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PharmaCompass offers a list of 6-Aminopenicillanic Acid 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 6-Aminopenicillanic Acid manufacturer or 6-Aminopenicillanic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 6-Aminopenicillanic Acid manufacturer or 6-Aminopenicillanic Acid supplier.
PharmaCompass also assists you with knowing the 6-Aminopenicillanic Acid API Price utilized in the formulation of products. 6-Aminopenicillanic Acid API Price is not always fixed or binding as the 6-Aminopenicillanic Acid Price is obtained through a variety of data sources. The 6-Aminopenicillanic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 6-Apa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6-Apa, including repackagers and relabelers. The FDA regulates 6-Apa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6-Apa 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 6-Apa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 6-Apa supplier is an individual or a company that provides 6-Apa active pharmaceutical ingredient (API) or 6-Apa finished formulations upon request. The 6-Apa suppliers may include 6-Apa API manufacturers, exporters, distributors and traders.
click here to find a list of 6-Apa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 6-Apa DMF (Drug Master File) is a document detailing the whole manufacturing process of 6-Apa active pharmaceutical ingredient (API) in detail. Different forms of 6-Apa DMFs exist exist since differing nations have different regulations, such as 6-Apa USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 6-Apa DMF submitted to regulatory agencies in the US is known as a USDMF. 6-Apa USDMF includes data on 6-Apa's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 6-Apa USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 6-Apa suppliers with USDMF 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 6-Apa as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 6-Apa 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 6-Apa 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 6-Apa and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 6-Apa NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 6-Apa suppliers with NDC on PharmaCompass.
6-Apa 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 6-Apa 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 6-Apa GMP manufacturer or 6-Apa GMP API supplier for your needs.
A 6-Apa CoA (Certificate of Analysis) is a formal document that attests to 6-Apa's compliance with 6-Apa specifications and serves as a tool for batch-level quality control.
6-Apa CoA mostly includes findings from lab analyses of a specific batch. For each 6-Apa 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.
6-Apa may be tested according to a variety of international standards, such as European Pharmacopoeia (6-Apa EP), 6-Apa JP (Japanese Pharmacopeia) and the US Pharmacopoeia (6-Apa USP).
