01 1Fine Chemicals Corporation (Pty) Limited
02 1Cambrex Charles City, Inc.
03 1SpecGx LLC
01 3Fentanyl
01 1Ireland
02 1South Africa
03 1U.S.A
Registration Number : 227MF10059
Registrant's Address : 15 Hawkins Avenue, Epping 1,7460, Cape Town, South Africa
Initial Date of Registration : 2015-03-06
Latest Date of Registration : 2024-03-13
Registration Number : 222MF10279
Registrant's Address : 1205 11th Street, Charles City, Iowa, U.S. S. A.
Initial Date of Registration : 2010-12-24
Latest Date of Registration : 2010-12-24
Registration Number : 221MF10283
Registrant's Address : 385 Marshall Ave, Webster Groves, Missouri 63119, United States
Initial Date of Registration : 2009-12-22
Latest Date of Registration : 2018-05-31
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PharmaCompass offers a list of Fentanyl 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 Fentanyl manufacturer or Fentanyl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fentanyl manufacturer or Fentanyl supplier.
PharmaCompass also assists you with knowing the Fentanyl API Price utilized in the formulation of products. Fentanyl API Price is not always fixed or binding as the Fentanyl Price is obtained through a variety of data sources. The Fentanyl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sublimaze manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sublimaze, including repackagers and relabelers. The FDA regulates Sublimaze manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sublimaze 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 Sublimaze manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sublimaze supplier is an individual or a company that provides Sublimaze active pharmaceutical ingredient (API) or Sublimaze finished formulations upon request. The Sublimaze suppliers may include Sublimaze API manufacturers, exporters, distributors and traders.
click here to find a list of Sublimaze 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 Sublimaze Drug Master File in Japan (Sublimaze JDMF) empowers Sublimaze 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 Sublimaze JDMF during the approval evaluation for pharmaceutical products. At the time of Sublimaze 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 Sublimaze suppliers with JDMF on PharmaCompass.
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