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PharmaCompass offers a list of Ibuprofen 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 Ibuprofen manufacturer or Ibuprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ibuprofen manufacturer or Ibuprofen supplier.
PharmaCompass also assists you with knowing the Ibuprofen API Price utilized in the formulation of products. Ibuprofen API Price is not always fixed or binding as the Ibuprofen Price is obtained through a variety of data sources. The Ibuprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nurofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nurofen, including repackagers and relabelers. The FDA regulates Nurofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nurofen 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 Nurofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nurofen supplier is an individual or a company that provides Nurofen active pharmaceutical ingredient (API) or Nurofen finished formulations upon request. The Nurofen suppliers may include Nurofen API manufacturers, exporters, distributors and traders.
click here to find a list of Nurofen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nurofen DMF (Drug Master File) is a document detailing the whole manufacturing process of Nurofen active pharmaceutical ingredient (API) in detail. Different forms of Nurofen DMFs exist exist since differing nations have different regulations, such as Nurofen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nurofen DMF submitted to regulatory agencies in the US is known as a USDMF. Nurofen USDMF includes data on Nurofen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nurofen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nurofen 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 Nurofen Drug Master File in Japan (Nurofen JDMF) empowers Nurofen 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 Nurofen JDMF during the approval evaluation for pharmaceutical products. At the time of Nurofen 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 Nurofen suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Nurofen Drug Master File in Korea (Nurofen KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nurofen. The MFDS reviews the Nurofen KDMF as part of the drug registration process and uses the information provided in the Nurofen KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nurofen KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Nurofen API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Nurofen suppliers with KDMF on PharmaCompass.
A Nurofen CEP of the European Pharmacopoeia monograph is often referred to as a Nurofen Certificate of Suitability (COS). The purpose of a Nurofen CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nurofen EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nurofen to their clients by showing that a Nurofen CEP has been issued for it. The manufacturer submits a Nurofen CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nurofen CEP holder for the record. Additionally, the data presented in the Nurofen CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nurofen DMF.
A Nurofen CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nurofen 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 Nurofen suppliers with CEP (COS) on PharmaCompass.
A Nurofen written confirmation (Nurofen WC) is an official document issued by a regulatory agency to a Nurofen manufacturer, verifying that the manufacturing facility of a Nurofen active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nurofen APIs or Nurofen finished pharmaceutical products to another nation, regulatory agencies frequently require a Nurofen WC (written confirmation) as part of the regulatory process.
click here to find a list of Nurofen suppliers with Written Confirmation (WC) 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 Nurofen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nurofen 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 Nurofen 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 Nurofen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nurofen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nurofen suppliers with NDC on PharmaCompass.
Nurofen 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 Nurofen 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 Nurofen GMP manufacturer or Nurofen GMP API supplier for your needs.
A Nurofen CoA (Certificate of Analysis) is a formal document that attests to Nurofen's compliance with Nurofen specifications and serves as a tool for batch-level quality control.
Nurofen CoA mostly includes findings from lab analyses of a specific batch. For each Nurofen 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.
Nurofen may be tested according to a variety of international standards, such as European Pharmacopoeia (Nurofen EP), Nurofen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nurofen USP).
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