01 1Ryoto Fine Co., Ltd.
02 2Sanyo Chemical Research Institute Co., Ltd.
03 1Tateyama Chemical Co., Ltd.
04 1Zhejiang Langhua Pharmaceutical Co. , Ltd.
01 2Ethyl Loflazepate
02 1Ethyl Loflazepate Intermediate
03 1Loflazepate ethyl
04 1Loflazepate ethyl "Tateyama"
01 1China
02 2Gabon
03 2Japan
Registration Number : 302MF10063
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2020-06-04
Latest Date of Registration : 2020-06-04
Registration Number : 228MF10042
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2016-02-08
Latest Date of Registration : 2016-02-08
Registration Number : 217MF10147
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2008-01-10
Registration Number : 301MF10016
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2019-06-07
Latest Date of Registration : 2019-06-07
Ethyl Loflazepate Intermediate
Registration Number : 302MF10056
Registrant's Address : Zhejiang provincial chemical and medical materials base Linhai zone, Linhai, Zhejiang...
Initial Date of Registration : 2020-05-12
Latest Date of Registration : 2020-05-12
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PharmaCompass offers a list of Ethyl Loflazepate 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 Ethyl Loflazepate manufacturer or Ethyl Loflazepate supplier for your needs.
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PharmaCompass also assists you with knowing the Ethyl Loflazepate API Price utilized in the formulation of products. Ethyl Loflazepate API Price is not always fixed or binding as the Ethyl Loflazepate Price is obtained through a variety of data sources. The Ethyl Loflazepate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Loflazepato de etilo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loflazepato de etilo, including repackagers and relabelers. The FDA regulates Loflazepato de etilo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loflazepato de etilo API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Loflazepato de etilo supplier is an individual or a company that provides Loflazepato de etilo active pharmaceutical ingredient (API) or Loflazepato de etilo finished formulations upon request. The Loflazepato de etilo suppliers may include Loflazepato de etilo API manufacturers, exporters, distributors and traders.
click here to find a list of Loflazepato de etilo 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 Loflazepato de etilo Drug Master File in Japan (Loflazepato de etilo JDMF) empowers Loflazepato de etilo 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 Loflazepato de etilo JDMF during the approval evaluation for pharmaceutical products. At the time of Loflazepato de etilo 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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