01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Verapamil Hydrochloride
01 1Italy
Registration Number : 230MF10106
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2018-08-08
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PharmaCompass offers a list of Verapamil Hydrochloride 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 Verapamil Hydrochloride manufacturer or Verapamil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Verapamil Hydrochloride manufacturer or Verapamil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Verapamil Hydrochloride API Price utilized in the formulation of products. Verapamil Hydrochloride API Price is not always fixed or binding as the Verapamil Hydrochloride Price is obtained through a variety of data sources. The Verapamil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cordilox SR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cordilox SR, including repackagers and relabelers. The FDA regulates Cordilox SR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cordilox SR 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 Cordilox SR manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cordilox SR supplier is an individual or a company that provides Cordilox SR active pharmaceutical ingredient (API) or Cordilox SR finished formulations upon request. The Cordilox SR suppliers may include Cordilox SR API manufacturers, exporters, distributors and traders.
click here to find a list of Cordilox SR 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 Cordilox SR Drug Master File in Japan (Cordilox SR JDMF) empowers Cordilox SR 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 Cordilox SR JDMF during the approval evaluation for pharmaceutical products. At the time of Cordilox SR 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 Cordilox SR suppliers with JDMF on PharmaCompass.
