01 1JQC (Huayin) Pharmaceutical Co. , Ltd.
02 1UBE Inc.
01 1Japanese Pharmacopoeia methyl salicylate
02 1Methyl salicylate
01 1China
02 1Japan
Registration Number : 217MF10869
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2009-07-23
Japanese Pharmacopoeia Methyl Salicylate
Registration Number : 222MF10143
Registrant's Address : YUQUAN ROAD,HUAYIN CITY,SHAANXI PROVINCE,714203,CHINA
Initial Date of Registration : 2010-04-20
Latest Date of Registration : 2010-04-20
A Methyl Salicylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyl Salicylate, including repackagers and relabelers. The FDA regulates Methyl Salicylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyl Salicylate 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 Methyl Salicylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyl Salicylate supplier is an individual or a company that provides Methyl Salicylate active pharmaceutical ingredient (API) or Methyl Salicylate finished formulations upon request. The Methyl Salicylate suppliers may include Methyl Salicylate API manufacturers, exporters, distributors and traders.
click here to find a list of Methyl Salicylate 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 Methyl Salicylate Drug Master File in Japan (Methyl Salicylate JDMF) empowers Methyl Salicylate 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 Methyl Salicylate JDMF during the approval evaluation for pharmaceutical products. At the time of Methyl Salicylate 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 Methyl Salicylate suppliers with JDMF on PharmaCompass.
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