Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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VMF
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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FDF
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
API SUPPLIERS
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
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USDMF
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API Imports and Exports
FDF Dossiers
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EUROAPI
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharm-RX Chemical
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shandong Focus Biotechnology Co., Ltd
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Shanghai Shenmei Pharmaceutical Technology Co., Ltd
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Fillers, Diluents & Binders
Solubilizers
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Coating Systems & Additives
Taste Masking
Parenteral
Controlled & Modified Release
Emulsifying Agents
Direct Compression
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Granulation
Disintegrants & Superdisintegrants
Lubricants & Glidants
Surfactant & Foaming Agents
Chewable & Orodispersible Aids
Co-Processed Excipients
Rheology Modifiers
API Stability Enhancers
Empty Capsules
Coloring Agents
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Soft Gelatin
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Avobenzona 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 Avobenzona manufacturer or Avobenzona supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Avobenzona manufacturer or Avobenzona supplier.
PharmaCompass also assists you with knowing the Avobenzona API Price utilized in the formulation of products. Avobenzona API Price is not always fixed or binding as the Avobenzona Price is obtained through a variety of data sources. The Avobenzona Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A avobenzone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of avobenzone, including repackagers and relabelers. The FDA regulates avobenzone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. avobenzone 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 avobenzone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A avobenzone supplier is an individual or a company that provides avobenzone active pharmaceutical ingredient (API) or avobenzone finished formulations upon request. The avobenzone suppliers may include avobenzone API manufacturers, exporters, distributors and traders.
click here to find a list of avobenzone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A avobenzone DMF (Drug Master File) is a document detailing the whole manufacturing process of avobenzone active pharmaceutical ingredient (API) in detail. Different forms of avobenzone DMFs exist exist since differing nations have different regulations, such as avobenzone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A avobenzone DMF submitted to regulatory agencies in the US is known as a USDMF. avobenzone USDMF includes data on avobenzone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The avobenzone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of avobenzone 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 avobenzone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for avobenzone 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 avobenzone 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 avobenzone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a avobenzone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of avobenzone suppliers with NDC on PharmaCompass.
avobenzone 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 avobenzone 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 avobenzone GMP manufacturer or avobenzone GMP API supplier for your needs.
A avobenzone CoA (Certificate of Analysis) is a formal document that attests to avobenzone's compliance with avobenzone specifications and serves as a tool for batch-level quality control.
avobenzone CoA mostly includes findings from lab analyses of a specific batch. For each avobenzone 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.
avobenzone may be tested according to a variety of international standards, such as European Pharmacopoeia (avobenzone EP), avobenzone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (avobenzone USP).
