01 1Excella GmbH & Co. K.G.
01 1Mianserin hydrochloride
01 1Luxembourg
Registration Number : 220MF10219
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2008-10-27
Latest Date of Registration : 2020-09-24
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PharmaCompass offers a list of Mianserin Hydrochloride 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 Mianserin Hydrochloride manufacturer or Mianserin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mianserin Hydrochloride manufacturer or Mianserin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Mianserin Hydrochloride API Price utilized in the formulation of products. Mianserin Hydrochloride API Price is not always fixed or binding as the Mianserin Hydrochloride Price is obtained through a variety of data sources. The Mianserin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tolvon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tolvon, including repackagers and relabelers. The FDA regulates Tolvon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tolvon 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 Tolvon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tolvon supplier is an individual or a company that provides Tolvon active pharmaceutical ingredient (API) or Tolvon finished formulations upon request. The Tolvon suppliers may include Tolvon API manufacturers, exporters, distributors and traders.
click here to find a list of Tolvon 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 Tolvon Drug Master File in Japan (Tolvon JDMF) empowers Tolvon 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 Tolvon JDMF during the approval evaluation for pharmaceutical products. At the time of Tolvon 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 Tolvon suppliers with JDMF on PharmaCompass.
