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