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.
01 9Celecoxib
02 1Celecoxib (manufacturing only)
01 6China
02 2India
03 2South Korea
Registration Number : 231MF10037
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2019-02-12
Latest Date of Registration : 2019-02-12
Registration Number : 230MF10110
Registrant's Address : Cipla House, Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel, Mumbai - 400...
Initial Date of Registration : 2018-08-20
Latest Date of Registration : 2018-08-20
Registration Number : 231MF10013
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2019-01-21
Latest Date of Registration : 2019-01-21
Registration Number : 231MF10035
Registrant's Address : No. 2 East Kangtai Road, Tangyin, Anyang, Henan, China
Initial Date of Registration : 2019-02-12
Latest Date of Registration : 2019-02-12
Registration Number : 231MF10025
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2019-02-05
Latest Date of Registration : 2019-02-05
Registration Number : 230MF10124
Registrant's Address : Jiangxi Fengxin Industrial Park, Fengxin, 330700, Jiangxi Province, P. R. China
Initial Date of Registration : 2018-09-03
Latest Date of Registration : 2018-09-03
Registration Number : 230MF10158
Registrant's Address : 161, Yeoksam-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2018-11-20
Latest Date of Registration : 2018-11-20
Registration Number : 231MF10046
Registrant's Address : No. 60 Taiyuan Rd. , Dajijia Industrial Park, YEDA Yantai, Shandong China
Initial Date of Registration : 2019-02-15
Latest Date of Registration : 2019-02-15
Japanese Pharmacopoeia Celecoxib (for manufacturing only)
Registration Number : 305MF10080
Registrant's Address : NO. 36 HUAYANG ROAD, HI-TECH INDUSTRY ZONE, QUZHOU CITY, ZHEJIANG, CHINA
Initial Date of Registration : 2023-07-12
Latest Date of Registration : 2023-07-12
Celecoxib (for manufacturing purposes only)
Registration Number : 302MF10050
Registrant's Address : NO. 36 HUAYANG ROAD, HI-TECH INDUSTRY ZONE, QUZHOU CITY, ZHEJIANG, CHINA
Initial Date of Registration : 2020-04-27
Latest Date of Registration : 2020-04-27
A Celebrex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celebrex, including repackagers and relabelers. The FDA regulates Celebrex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celebrex 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 Celebrex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Celebrex supplier is an individual or a company that provides Celebrex active pharmaceutical ingredient (API) or Celebrex finished formulations upon request. The Celebrex suppliers may include Celebrex API manufacturers, exporters, distributors and traders.
click here to find a list of Celebrex 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 Celebrex Drug Master File in Japan (Celebrex JDMF) empowers Celebrex 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 Celebrex JDMF during the approval evaluation for pharmaceutical products. At the time of Celebrex 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 Celebrex suppliers with JDMF on PharmaCompass.
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