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.
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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 Norfenazin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Norfenazin, including repackagers and relabelers. The FDA regulates Norfenazin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Norfenazin 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 Norfenazin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Norfenazin supplier is an individual or a company that provides Norfenazin active pharmaceutical ingredient (API) or Norfenazin finished formulations upon request. The Norfenazin suppliers may include Norfenazin API manufacturers, exporters, distributors and traders.
click here to find a list of Norfenazin 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 Norfenazin Drug Master File in Japan (Norfenazin JDMF) empowers Norfenazin 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 Norfenazin JDMF during the approval evaluation for pharmaceutical products. At the time of Norfenazin 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 Norfenazin suppliers with JDMF on PharmaCompass.
