X
API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
EU WC
0
Listed Suppliers
0
USA (Orange Book)
0
Europe
Canada
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
0
21
PharmaCompass offers a list of Salicylic 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 Salicylic Acid manufacturer or Salicylic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Salicylic Acid manufacturer or Salicylic Acid supplier.
PharmaCompass also assists you with knowing the Salicylic Acid API Price utilized in the formulation of products. Salicylic Acid API Price is not always fixed or binding as the Salicylic Acid Price is obtained through a variety of data sources. The Salicylic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Salicylic acid-ring-UL-14C manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicylic acid-ring-UL-14C, including repackagers and relabelers. The FDA regulates Salicylic acid-ring-UL-14C manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicylic acid-ring-UL-14C supplier is an individual or a company that provides Salicylic acid-ring-UL-14C active pharmaceutical ingredient (API) or Salicylic acid-ring-UL-14C finished formulations upon request. The Salicylic acid-ring-UL-14C suppliers may include Salicylic acid-ring-UL-14C API manufacturers, exporters, distributors and traders.
click here to find a list of Salicylic acid-ring-UL-14C suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Salicylic acid-ring-UL-14C DMF (Drug Master File) is a document detailing the whole manufacturing process of Salicylic acid-ring-UL-14C active pharmaceutical ingredient (API) in detail. Different forms of Salicylic acid-ring-UL-14C DMFs exist exist since differing nations have different regulations, such as Salicylic acid-ring-UL-14C USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Salicylic acid-ring-UL-14C DMF submitted to regulatory agencies in the US is known as a USDMF. Salicylic acid-ring-UL-14C USDMF includes data on Salicylic acid-ring-UL-14C's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Salicylic acid-ring-UL-14C USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C Drug Master File in Japan (Salicylic acid-ring-UL-14C JDMF) empowers Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C JDMF during the approval evaluation for pharmaceutical products. At the time of Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C suppliers with JDMF on PharmaCompass.
A Salicylic acid-ring-UL-14C CEP of the European Pharmacopoeia monograph is often referred to as a Salicylic acid-ring-UL-14C Certificate of Suitability (COS). The purpose of a Salicylic acid-ring-UL-14C CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Salicylic acid-ring-UL-14C EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Salicylic acid-ring-UL-14C to their clients by showing that a Salicylic acid-ring-UL-14C CEP has been issued for it. The manufacturer submits a Salicylic acid-ring-UL-14C CEP (COS) as part of the market authorization procedure, and it takes on the role of a Salicylic acid-ring-UL-14C CEP holder for the record. Additionally, the data presented in the Salicylic acid-ring-UL-14C CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Salicylic acid-ring-UL-14C DMF.
A Salicylic acid-ring-UL-14C CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Salicylic acid-ring-UL-14C NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Salicylic acid-ring-UL-14C suppliers with NDC on PharmaCompass.
Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C 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 Salicylic acid-ring-UL-14C GMP manufacturer or Salicylic acid-ring-UL-14C GMP API supplier for your needs.
A Salicylic acid-ring-UL-14C CoA (Certificate of Analysis) is a formal document that attests to Salicylic acid-ring-UL-14C's compliance with Salicylic acid-ring-UL-14C specifications and serves as a tool for batch-level quality control.
Salicylic acid-ring-UL-14C CoA mostly includes findings from lab analyses of a specific batch. For each Salicylic acid-ring-UL-14C 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.
Salicylic acid-ring-UL-14C may be tested according to a variety of international standards, such as European Pharmacopoeia (Salicylic acid-ring-UL-14C EP), Salicylic acid-ring-UL-14C JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Salicylic acid-ring-UL-14C USP).
Market Place
