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01 1SANOFI WINTHROP INDUSTRIE
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01 1Naloxone hydrochloride hydrate
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01 1France
Naloxone hydrochloride hydrate
Registration Number : 218MF10971
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2019-03-19
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PharmaCompass offers a list of Naloxone 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 Naloxone Hydrochloride manufacturer or Naloxone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naloxone Hydrochloride manufacturer or Naloxone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Naloxone Hydrochloride API Price utilized in the formulation of products. Naloxone Hydrochloride API Price is not always fixed or binding as the Naloxone Hydrochloride Price is obtained through a variety of data sources. The Naloxone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Naloxone Hydrochloride Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naloxone Hydrochloride Dihydrate, including repackagers and relabelers. The FDA regulates Naloxone Hydrochloride Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naloxone Hydrochloride Dihydrate supplier is an individual or a company that provides Naloxone Hydrochloride Dihydrate active pharmaceutical ingredient (API) or Naloxone Hydrochloride Dihydrate finished formulations upon request. The Naloxone Hydrochloride Dihydrate suppliers may include Naloxone Hydrochloride Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate Drug Master File in Japan (Naloxone Hydrochloride Dihydrate JDMF) empowers Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Naloxone Hydrochloride Dihydrate 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 Naloxone Hydrochloride Dihydrate suppliers with JDMF on PharmaCompass.
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