01 1Baoji Tianxin Pharmaceutical Co. , Ltd.
02 2Cheng Fong Chemical Co. , Ltd.
03 3Yamamoto Chemical Industry Co., Ltd.
01 1Day stations mefenamic acid (production only)
02 3Japanese Pharmacopoeia mefenamic acid
03 1Mefenamic acid
04 1Mefenamic acid M
01 3China
02 3Japan
Registration Number : 230MF10054
Registrant's Address : 16F. , No. 3, Park St. , Nangang Dist. , Taipei City 115, Taiwan (R.O.C.)
Initial Date of Registration : 2018-04-17
Latest Date of Registration : 2018-10-01
Japanese Pharmacopoeia Mefenamic Acid (for manufacturing purposes only)
Registration Number : 218MF10062
Registrant's Address : 16F. , No. 3, Park St. , Nangang Dist. , Taipei City 115, Taiwan (R.O.C.)
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2018-09-06
Registration Number : 224MF10137
Registrant's Address : Caijiapo Economic & Technical Development Zone, Qishan County, Shaanxi Province, Chin...
Initial Date of Registration : 2012-07-30
Latest Date of Registration : 2012-07-30
Japanese Pharmacopoeia Mefenamic Acid
Registration Number : 225MF10024
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2013-02-13
Japanese Pharmacopoeia Mefenamic Acid
Registration Number : 222MF10243
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2010-10-13
Latest Date of Registration : 2010-10-13
Japanese Pharmacopoeia Mefenamic Acid
Registration Number : 217MF10557
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-12-19
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PharmaCompass offers a list of Mefenamic Acid 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 Mefenamic Acid manufacturer or Mefenamic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mefenamic Acid manufacturer or Mefenamic Acid supplier.
PharmaCompass also assists you with knowing the Mefenamic Acid API Price utilized in the formulation of products. Mefenamic Acid API Price is not always fixed or binding as the Mefenamic Acid Price is obtained through a variety of data sources. The Mefenamic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lysalgo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lysalgo, including repackagers and relabelers. The FDA regulates Lysalgo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lysalgo 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 Lysalgo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lysalgo supplier is an individual or a company that provides Lysalgo active pharmaceutical ingredient (API) or Lysalgo finished formulations upon request. The Lysalgo suppliers may include Lysalgo API manufacturers, exporters, distributors and traders.
click here to find a list of Lysalgo 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 Lysalgo Drug Master File in Japan (Lysalgo JDMF) empowers Lysalgo 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 Lysalgo JDMF during the approval evaluation for pharmaceutical products. At the time of Lysalgo JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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