01 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
01 1Japanese Pharmacopoeia Etilefrine Hydrochloride Manufacturing Dedicated
01 1Japan
Japanese Pharmacopoeia Etilefrine Hydrochloride For manufacturing only
Registration Number : 305MF10005
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2023-01-18
Latest Date of Registration : 2024-02-07
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PharmaCompass offers a list of Etilefrine 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 Etilefrine manufacturer or Etilefrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etilefrine manufacturer or Etilefrine supplier.
PharmaCompass also assists you with knowing the Etilefrine API Price utilized in the formulation of products. Etilefrine API Price is not always fixed or binding as the Etilefrine Price is obtained through a variety of data sources. The Etilefrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Etilefrine Pivalate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etilefrine Pivalate Hydrochloride, including repackagers and relabelers. The FDA regulates Etilefrine Pivalate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etilefrine Pivalate Hydrochloride 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 Etilefrine Pivalate Hydrochloride supplier is an individual or a company that provides Etilefrine Pivalate Hydrochloride active pharmaceutical ingredient (API) or Etilefrine Pivalate Hydrochloride finished formulations upon request. The Etilefrine Pivalate Hydrochloride suppliers may include Etilefrine Pivalate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Etilefrine Pivalate Hydrochloride 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 Etilefrine Pivalate Hydrochloride Drug Master File in Japan (Etilefrine Pivalate Hydrochloride JDMF) empowers Etilefrine Pivalate Hydrochloride 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 Etilefrine Pivalate Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Etilefrine Pivalate Hydrochloride 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 Etilefrine Pivalate Hydrochloride suppliers with JDMF on PharmaCompass.
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