01 1Hebei Jingye Medical Technology Corp. , LTD. ,Coastal Port Pharmaceutical Branch
02 1Yamamoto Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia Aspirin
02 1Japanese Pharmacopoeia aspirin
01 1China
02 1Japan
Japanese Pharmacopoeia Aspirin
Registration Number : 301MF10041
Registrant's Address : East of Jingyi Road, West zone, Coastal-port economic technology development zone, Ca...
Initial Date of Registration : 2019-08-09
Latest Date of Registration : 2019-08-09
Japanese Pharmacopoeia Aspirin
Registration Number : 217MF10562
Registrant's Address : 1-4 Funatsu-cho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-07-17
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PharmaCompass offers a list of Aspirin 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 Aspirin manufacturer or Aspirin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aspirin manufacturer or Aspirin supplier.
A Endosprin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Endosprin, including repackagers and relabelers. The FDA regulates Endosprin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Endosprin 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 Endosprin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Endosprin supplier is an individual or a company that provides Endosprin active pharmaceutical ingredient (API) or Endosprin finished formulations upon request. The Endosprin suppliers may include Endosprin API manufacturers, exporters, distributors and traders.
click here to find a list of Endosprin 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 Endosprin Drug Master File in Japan (Endosprin JDMF) empowers Endosprin 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 Endosprin JDMF during the approval evaluation for pharmaceutical products. At the time of Endosprin 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 Endosprin suppliers with JDMF on PharmaCompass.
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