01 1Olon S. p. A.
01 1Maprotiline hydrochloride
01 1Italy
Registration Number : 219MF10106
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2020-01-10
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PharmaCompass offers a list of MAPROTILINE 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 MAPROTILINE HYDROCHLORIDE manufacturer or MAPROTILINE HYDROCHLORIDE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred MAPROTILINE HYDROCHLORIDE manufacturer or MAPROTILINE HYDROCHLORIDE supplier.
PharmaCompass also assists you with knowing the MAPROTILINE HYDROCHLORIDE API Price utilized in the formulation of products. MAPROTILINE HYDROCHLORIDE API Price is not always fixed or binding as the MAPROTILINE HYDROCHLORIDE Price is obtained through a variety of data sources. The MAPROTILINE HYDROCHLORIDE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deprilept manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deprilept, including repackagers and relabelers. The FDA regulates Deprilept manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deprilept 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 Deprilept manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deprilept supplier is an individual or a company that provides Deprilept active pharmaceutical ingredient (API) or Deprilept finished formulations upon request. The Deprilept suppliers may include Deprilept API manufacturers, exporters, distributors and traders.
click here to find a list of Deprilept 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 Deprilept Drug Master File in Japan (Deprilept JDMF) empowers Deprilept 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 Deprilept JDMF during the approval evaluation for pharmaceutical products. At the time of Deprilept 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 Deprilept suppliers with JDMF on PharmaCompass.
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