01 1Daiichi Sankyo Propharma Co., Ltd.
01 1Hydromorphone hydrochloride
01 1Japan
Registration Number : 227MF10256
Registrant's Address : 3-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2015-10-21
Latest Date of Registration : 2017-02-08
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PharmaCompass offers a list of Hydromorphone 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 Hydromorphone Hydrochloride manufacturer or Hydromorphone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydromorphone Hydrochloride manufacturer or Hydromorphone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Hydromorphone Hydrochloride API Price utilized in the formulation of products. Hydromorphone Hydrochloride API Price is not always fixed or binding as the Hydromorphone Hydrochloride Price is obtained through a variety of data sources. The Hydromorphone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydromorphon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydromorphon, including repackagers and relabelers. The FDA regulates Hydromorphon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydromorphon 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 Hydromorphon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydromorphon supplier is an individual or a company that provides Hydromorphon active pharmaceutical ingredient (API) or Hydromorphon finished formulations upon request. The Hydromorphon suppliers may include Hydromorphon API manufacturers, exporters, distributors and traders.
click here to find a list of Hydromorphon 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 Hydromorphon Drug Master File in Japan (Hydromorphon JDMF) empowers Hydromorphon 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 Hydromorphon JDMF during the approval evaluation for pharmaceutical products. At the time of Hydromorphon 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 Hydromorphon suppliers with JDMF on PharmaCompass.
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