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API SUPPLIERS
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 10% (10GM/100...DOSAGE - INJECTABLE;INJECTION - 10% (10GM/100ML)
USFDA APPLICATION NUMBER - 19018
DOSAGE - INJECTABLE;INJECTION - 6% (6GM/100ML...DOSAGE - INJECTABLE;INJECTION - 6% (6GM/100ML)
USFDA APPLICATION NUMBER - 19018
DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100...DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100ML;6.8GM/100ML;68MG/100ML;124MG/100ML;170MG/100ML;105MG/100ML;3.5GM/100ML (1440ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100...DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100ML;6.8GM/100ML;68MG/100ML;124MG/100ML;170MG/100ML;105MG/100ML;3.5GM/100ML (1920ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100...DOSAGE - EMULSION;INTRAVENOUS - 2.4%;20MG/100ML;6.8GM/100ML;68MG/100ML;124MG/100ML;170MG/100ML ;105MG/100ML;3.5GM/100ML (2400ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100...DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML ;147MG/100ML;3.9GM/100ML (1026ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100...DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (1540ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100...DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2053ML)
USFDA APPLICATION NUMBER - 200656
DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100...DOSAGE - EMULSION;INTRAVENOUS - 3.3%;29MG/100ML;9.8GM/100ML;96MG/100ML;174MG/100ML;239MG/100ML;147MG/100ML;3.9GM/100ML (2566ML)
USFDA APPLICATION NUMBER - 200656
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PharmaCompass offers a list of Amino Acids Mixture 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 Amino Acids Mixture manufacturer or Amino Acids Mixture supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amino Acids Mixture manufacturer or Amino Acids Mixture supplier.
PharmaCompass also assists you with knowing the Amino Acids Mixture API Price utilized in the formulation of products. Amino Acids Mixture API Price is not always fixed or binding as the Amino Acids Mixture Price is obtained through a variety of data sources. The Amino Acids Mixture Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AMINOSYN 10% manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMINOSYN 10%, including repackagers and relabelers. The FDA regulates AMINOSYN 10% manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMINOSYN 10% 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 AMINOSYN 10% manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AMINOSYN 10% supplier is an individual or a company that provides AMINOSYN 10% active pharmaceutical ingredient (API) or AMINOSYN 10% finished formulations upon request. The AMINOSYN 10% suppliers may include AMINOSYN 10% API manufacturers, exporters, distributors and traders.
click here to find a list of AMINOSYN 10% suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AMINOSYN 10% DMF (Drug Master File) is a document detailing the whole manufacturing process of AMINOSYN 10% active pharmaceutical ingredient (API) in detail. Different forms of AMINOSYN 10% DMFs exist exist since differing nations have different regulations, such as AMINOSYN 10% USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AMINOSYN 10% DMF submitted to regulatory agencies in the US is known as a USDMF. AMINOSYN 10% USDMF includes data on AMINOSYN 10%'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AMINOSYN 10% USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AMINOSYN 10% suppliers with USDMF on PharmaCompass.
A AMINOSYN 10% CEP of the European Pharmacopoeia monograph is often referred to as a AMINOSYN 10% Certificate of Suitability (COS). The purpose of a AMINOSYN 10% CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AMINOSYN 10% EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AMINOSYN 10% to their clients by showing that a AMINOSYN 10% CEP has been issued for it. The manufacturer submits a AMINOSYN 10% CEP (COS) as part of the market authorization procedure, and it takes on the role of a AMINOSYN 10% CEP holder for the record. Additionally, the data presented in the AMINOSYN 10% CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AMINOSYN 10% DMF.
A AMINOSYN 10% CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AMINOSYN 10% 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 AMINOSYN 10% suppliers with CEP (COS) 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 AMINOSYN 10% as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AMINOSYN 10% 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 AMINOSYN 10% 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 AMINOSYN 10% and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AMINOSYN 10% NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of AMINOSYN 10% suppliers with NDC on PharmaCompass.
AMINOSYN 10% 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 AMINOSYN 10% 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 AMINOSYN 10% GMP manufacturer or AMINOSYN 10% GMP API supplier for your needs.
A AMINOSYN 10% CoA (Certificate of Analysis) is a formal document that attests to AMINOSYN 10%'s compliance with AMINOSYN 10% specifications and serves as a tool for batch-level quality control.
AMINOSYN 10% CoA mostly includes findings from lab analyses of a specific batch. For each AMINOSYN 10% 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.
AMINOSYN 10% may be tested according to a variety of international standards, such as European Pharmacopoeia (AMINOSYN 10% EP), AMINOSYN 10% JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AMINOSYN 10% USP).
