01 1Arevipharma GmbH
02 1Kern Pharma, S. L.
03 2SpecGx LLC
01 1Fentanyl Citrate
02 2Fentanyl citrate
03 1Fentanyl citrate FP
01 1Germany
02 2Ireland
03 1Spain
Registration Number : 306MF10148
Registrant's Address : Meissner Strasse 35 D-01445 Radebeul, Germany
Initial Date of Registration : 2024-11-20
Latest Date of Registration : 2024-11-20
Registration Number : 226MF10217
Registrant's Address : Pol. Ind. Colo(´)n II Venus, 72 08228 Terrassa (Barcelona)-Spain
Initial Date of Registration : 2014-11-17
Latest Date of Registration : 2022-06-01
Registration Number : 229MF10161
Registrant's Address : 385 Marshall Ave, Webster Groves, Missouri 63119, United States
Initial Date of Registration : 2017-08-17
Latest Date of Registration : 2017-08-17
Registration Number : 218MF10580
Registrant's Address : 385 Marshall Ave, Webster Groves, Missouri 63119, United States
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2006-06-22
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PharmaCompass offers a list of Fentanyl Citrate 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 Citrate manufacturer or Fentanyl Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fentanyl Citrate manufacturer or Fentanyl Citrate supplier.
PharmaCompass also assists you with knowing the Fentanyl Citrate API Price utilized in the formulation of products. Fentanyl Citrate API Price is not always fixed or binding as the Fentanyl Citrate Price is obtained through a variety of data sources. The Fentanyl Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A INNOVAR-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of INNOVAR-1, including repackagers and relabelers. The FDA regulates INNOVAR-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. INNOVAR-1 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 INNOVAR-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A INNOVAR-1 supplier is an individual or a company that provides INNOVAR-1 active pharmaceutical ingredient (API) or INNOVAR-1 finished formulations upon request. The INNOVAR-1 suppliers may include INNOVAR-1 API manufacturers, exporters, distributors and traders.
click here to find a list of INNOVAR-1 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 INNOVAR-1 Drug Master File in Japan (INNOVAR-1 JDMF) empowers INNOVAR-1 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 INNOVAR-1 JDMF during the approval evaluation for pharmaceutical products. At the time of INNOVAR-1 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 INNOVAR-1 suppliers with JDMF on PharmaCompass.
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