API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
Other Certificates
Other Suppliers
USA (Orange Book)
Europe
Canada
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
Annual Reports
22
PharmaCompass offers a list of Ketoprofen 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 Ketoprofen manufacturer or Ketoprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ketoprofen manufacturer or Ketoprofen supplier.
PharmaCompass also assists you with knowing the Ketoprofen API Price utilized in the formulation of products. Ketoprofen API Price is not always fixed or binding as the Ketoprofen Price is obtained through a variety of data sources. The Ketoprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060549 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060549, including repackagers and relabelers. The FDA regulates AM20060549 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060549 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 AM20060549 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AM20060549 supplier is an individual or a company that provides AM20060549 active pharmaceutical ingredient (API) or AM20060549 finished formulations upon request. The AM20060549 suppliers may include AM20060549 API manufacturers, exporters, distributors and traders.
click here to find a list of AM20060549 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 AM20060549 Drug Master File in Japan (AM20060549 JDMF) empowers AM20060549 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 AM20060549 JDMF during the approval evaluation for pharmaceutical products. At the time of AM20060549 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 AM20060549 suppliers with JDMF on PharmaCompass.
We have 11 companies offering AM20060549
Get in contact with the supplier of your choice: