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
27
PharmaCompass offers a list of Fentanyl API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, 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.
A Durotep MT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Durotep MT, including repackagers and relabelers. The FDA regulates Durotep MT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Durotep MT 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 Durotep MT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Durotep MT supplier is an individual or a company that provides Durotep MT active pharmaceutical ingredient (API) or Durotep MT finished formulations upon request. The Durotep MT suppliers may include Durotep MT API manufacturers, exporters, distributors and traders.
click here to find a list of Durotep MT suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Durotep MT Drug Master File in Japan (Durotep MT JDMF) empowers Durotep MT 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 Durotep MT JDMF during the approval evaluation for pharmaceutical products. At the time of Durotep MT 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 Durotep MT suppliers with JDMF on PharmaCompass.
We have 3 companies offering Durotep MT
Get in contact with the supplier of your choice:
