01 1Dipharma Francis S. r. l.
01 1Nortriptyline hydrochloride
01 1Italy
Registration Number : 219MF10264
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2007-08-16
Latest Date of Registration : 2021-05-24
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PharmaCompass offers a list of Nortriptyline 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 Nortriptyline manufacturer or Nortriptyline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nortriptyline manufacturer or Nortriptyline supplier.
PharmaCompass also assists you with knowing the Nortriptyline API Price utilized in the formulation of products. Nortriptyline API Price is not always fixed or binding as the Nortriptyline Price is obtained through a variety of data sources. The Nortriptyline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aventyl allegron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aventyl allegron, including repackagers and relabelers. The FDA regulates Aventyl allegron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aventyl allegron 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 Aventyl allegron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aventyl allegron supplier is an individual or a company that provides Aventyl allegron active pharmaceutical ingredient (API) or Aventyl allegron finished formulations upon request. The Aventyl allegron suppliers may include Aventyl allegron API manufacturers, exporters, distributors and traders.
click here to find a list of Aventyl allegron 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 Aventyl allegron Drug Master File in Japan (Aventyl allegron JDMF) empowers Aventyl allegron 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 Aventyl allegron JDMF during the approval evaluation for pharmaceutical products. At the time of Aventyl allegron 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 Aventyl allegron suppliers with JDMF on PharmaCompass.
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