01 1H. Lundbeck A/S
02 1Lundbeck Pharmaceuticals Italy S. p. A
01 2Nalmefene hydrochloride hydrate
01 2Denmark
Nalmefene hydrochloride hydrate
Registration Number : 229MF10110
Registrant's Address : Via Quarta Strada, 2 Padova, Italy
Initial Date of Registration : 2017-06-26
Latest Date of Registration : 2018-07-03
Nalmefene hydrochloride hydrate
Registration Number : 229MF10109
Registrant's Address : Ottiliavej 9, DK-2500 Valby, Copenhagen, Denmark
Initial Date of Registration : 2017-06-26
Latest Date of Registration : 2018-07-03
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PharmaCompass offers a list of Nalmefene 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 Nalmefene Hydrochloride manufacturer or Nalmefene Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Nalmefene Hydrochloride API Price utilized in the formulation of products. Nalmefene Hydrochloride API Price is not always fixed or binding as the Nalmefene Hydrochloride Price is obtained through a variety of data sources. The Nalmefene Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nalmefene HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nalmefene HCl, including repackagers and relabelers. The FDA regulates Nalmefene HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nalmefene HCl 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 Nalmefene HCl supplier is an individual or a company that provides Nalmefene HCl active pharmaceutical ingredient (API) or Nalmefene HCl finished formulations upon request. The Nalmefene HCl suppliers may include Nalmefene HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Nalmefene HCl 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 Nalmefene HCl Drug Master File in Japan (Nalmefene HCl JDMF) empowers Nalmefene HCl 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 Nalmefene HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Nalmefene HCl 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 Nalmefene HCl suppliers with JDMF on PharmaCompass.
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