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 Manidon Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Manidon Retard, including repackagers and relabelers. The FDA regulates Manidon Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Manidon Retard 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 Manidon Retard supplier is an individual or a company that provides Manidon Retard active pharmaceutical ingredient (API) or Manidon Retard finished formulations upon request. The Manidon Retard suppliers may include Manidon Retard API manufacturers, exporters, distributors and traders.
click here to find a list of Manidon Retard 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 Manidon Retard Drug Master File in Japan (Manidon Retard JDMF) empowers Manidon Retard 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 Manidon Retard JDMF during the approval evaluation for pharmaceutical products. At the time of Manidon Retard 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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