01 1AMSA S. p. A.
02 1CADILA PHARMACEUTICALS LIMITED.
03 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
04 1Derivados Quimicos sau
05 1Hwail Pharmaceutical Co. , Ltd.
06 1Ilshin Chemical Co. , Ltd.
07 2UNICHEM LABORATORIES LIMITED.
01 1MELOXICAM
02 6Meloxicam
03 1Meloxicam (production only)
01 3India
02 1Italy
03 3South Korea
04 1Spain
Registration Number : 218MF11036
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2018-09-21
Meloxicam (for manufacturing purposes only)
Registration Number : 226MF10171
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-09-01
Registration Number : 218MF10765
Registrant's Address : Camino Viejo de Pliego, s/n 30820 Alcantarilla Murcia Spain
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2016-08-03
Registration Number : 219MF10075
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
Registration Number : 219MF10033
Registrant's Address : 57, Jeyakgongdan 3-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2007-02-05
Latest Date of Registration : 2007-02-05
Registration Number : 219MF10072
Registrant's Address : 1074, YANGSAN-DAERO, YANGSAN-SI, GYEONGSANGNAM-DO, KOREA
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
Registration Number : 307MF10023
Registrant's Address : 47, Kandivli Industrial Estate, Kandivli (West), Mumbai-400067, Maharashtra, India
Initial Date of Registration : 2025-01-28
Latest Date of Registration : 2025-01-28
Registration Number : 219MF10088
Registrant's Address : Unichem Bhavan, Prabhat Estate, S. V. Road, Jogeshwari (West), Mumbai-400 102, India
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2021-04-02
27
PharmaCompass offers a list of Meloxicam 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 Meloxicam manufacturer or Meloxicam supplier for your needs.
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PharmaCompass also assists you with knowing the Meloxicam API Price utilized in the formulation of products. Meloxicam API Price is not always fixed or binding as the Meloxicam Price is obtained through a variety of data sources. The Meloxicam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Artriflam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Artriflam, including repackagers and relabelers. The FDA regulates Artriflam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Artriflam 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 Artriflam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Artriflam supplier is an individual or a company that provides Artriflam active pharmaceutical ingredient (API) or Artriflam finished formulations upon request. The Artriflam suppliers may include Artriflam API manufacturers, exporters, distributors and traders.
click here to find a list of Artriflam 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 Artriflam Drug Master File in Japan (Artriflam JDMF) empowers Artriflam 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 Artriflam JDMF during the approval evaluation for pharmaceutical products. At the time of Artriflam 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 Artriflam suppliers with JDMF on PharmaCompass.
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