01 1Dipharma Francis S. r. l.
01 1Cyclobenzaprine Hydrochloride
01 1Italy
Registration Number : 306MF10003
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2024-01-11
Latest Date of Registration : 2024-01-11
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PharmaCompass offers a list of Cyclobenzaprine 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 Cyclobenzaprine manufacturer or Cyclobenzaprine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclobenzaprine manufacturer or Cyclobenzaprine supplier.
PharmaCompass also assists you with knowing the Cyclobenzaprine API Price utilized in the formulation of products. Cyclobenzaprine API Price is not always fixed or binding as the Cyclobenzaprine Price is obtained through a variety of data sources. The Cyclobenzaprine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flexiban manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flexiban, including repackagers and relabelers. The FDA regulates Flexiban manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flexiban API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Flexiban supplier is an individual or a company that provides Flexiban active pharmaceutical ingredient (API) or Flexiban finished formulations upon request. The Flexiban suppliers may include Flexiban API manufacturers, exporters, distributors and traders.
click here to find a list of Flexiban 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 Flexiban Drug Master File in Japan (Flexiban JDMF) empowers Flexiban 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 Flexiban JDMF during the approval evaluation for pharmaceutical products. At the time of Flexiban JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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