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PharmaCompass offers a list of Celecoxib 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 Celecoxib manufacturer or Celecoxib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Celecoxib manufacturer or Celecoxib supplier.
PharmaCompass also assists you with knowing the Celecoxib API Price utilized in the formulation of products. Celecoxib API Price is not always fixed or binding as the Celecoxib Price is obtained through a variety of data sources. The Celecoxib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Celecoxib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celecoxib, including repackagers and relabelers. The FDA regulates Celecoxib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celecoxib 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 Celecoxib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Celecoxib supplier is an individual or a company that provides Celecoxib active pharmaceutical ingredient (API) or Celecoxib finished formulations upon request. The Celecoxib suppliers may include Celecoxib API manufacturers, exporters, distributors and traders.
click here to find a list of Celecoxib 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 Celecoxib Drug Master File in Japan (Celecoxib JDMF) empowers Celecoxib 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 Celecoxib JDMF during the approval evaluation for pharmaceutical products. At the time of Celecoxib 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 Celecoxib suppliers with JDMF on PharmaCompass.
We have 10 companies offering Celecoxib
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