01 1Ryoto Fine Co., Ltd.
02 1Tateyama Chemical Co., Ltd.
03 1Zhejiang Langhua Pharmaceutical Co. , Ltd.
01 1Ethyl Loflazepate
02 1Ethyl Loflazepate Intermediate
03 1Loflazepate ethyl "Tateyama"
01 1China
02 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
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethyl Loflazepate manufacturer or Ethyl Loflazepate supplier.
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 Ethyl Loflazepate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethyl Loflazepate, including repackagers and relabelers. The FDA regulates Ethyl Loflazepate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethyl Loflazepate 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 Ethyl Loflazepate supplier is an individual or a company that provides Ethyl Loflazepate active pharmaceutical ingredient (API) or Ethyl Loflazepate finished formulations upon request. The Ethyl Loflazepate suppliers may include Ethyl Loflazepate API manufacturers, exporters, distributors and traders.
click here to find a list of Ethyl Loflazepate 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 Ethyl Loflazepate Drug Master File in Japan (Ethyl Loflazepate JDMF) empowers Ethyl Loflazepate 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 Ethyl Loflazepate JDMF during the approval evaluation for pharmaceutical products. At the time of Ethyl Loflazepate 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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