Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
01 1COSMA S. P. A.
01 1Hydroxy Jinpa model salt
01 1Italy
Cosma S.p.A.: FDA-approved API manufacturing with 300+ tons capacity, serving pharma and animal health industries worldwide.
Registration Number : 218MF11037
Registrant's Address : Via Colleoni 15/17, 24040 Ciserano(BG)・Italy
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2021-10-21
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PharmaCompass offers a list of Hydroxyzine Pamoate 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 Hydroxyzine Pamoate manufacturer or Hydroxyzine Pamoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroxyzine Pamoate manufacturer or Hydroxyzine Pamoate supplier.
PharmaCompass also assists you with knowing the Hydroxyzine Pamoate API Price utilized in the formulation of products. Hydroxyzine Pamoate API Price is not always fixed or binding as the Hydroxyzine Pamoate Price is obtained through a variety of data sources. The Hydroxyzine Pamoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hy-Pam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hy-Pam, including repackagers and relabelers. The FDA regulates Hy-Pam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hy-Pam 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 Hy-Pam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hy-Pam supplier is an individual or a company that provides Hy-Pam active pharmaceutical ingredient (API) or Hy-Pam finished formulations upon request. The Hy-Pam suppliers may include Hy-Pam API manufacturers, exporters, distributors and traders.
click here to find a list of Hy-Pam 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 Hy-Pam Drug Master File in Japan (Hy-Pam JDMF) empowers Hy-Pam 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 Hy-Pam JDMF during the approval evaluation for pharmaceutical products. At the time of Hy-Pam 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 Hy-Pam suppliers with JDMF on PharmaCompass.
