01 1Cheer Fine Pharmaceutical Co. , Ltd.
02 1Cipla Limited
03 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 1HENAN DONGTAI PHARM CO. , LTD.
05 1HETERO DRUGS LIMITED.
06 1Jiangxi Synergy Pharmaceutical Co. , Ltd.
07 1Shin Poong Pharm. Co. , Ltd.
08 1Yantai Valiant Pharmaceutical Co. , Ltd.
09 2ZHEJIANG CHEMSYN PHARM CO. , LTD.
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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, 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.
A Medicoxib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Medicoxib, including repackagers and relabelers. The FDA regulates Medicoxib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Medicoxib 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 Medicoxib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Medicoxib supplier is an individual or a company that provides Medicoxib active pharmaceutical ingredient (API) or Medicoxib finished formulations upon request. The Medicoxib suppliers may include Medicoxib API manufacturers, exporters, distributors and traders.
click here to find a list of Medicoxib suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Medicoxib Drug Master File in Japan (Medicoxib JDMF) empowers Medicoxib 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 Medicoxib JDMF during the approval evaluation for pharmaceutical products. At the time of Medicoxib 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 Medicoxib suppliers with JDMF on PharmaCompass.
We have 9 companies offering Medicoxib
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