01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Papaverine Hydrochloride
01 1Italy
Registration Number : 231MF10018
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2019-01-29
Latest Date of Registration : 2019-01-29
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PharmaCompass offers a list of Papaverine 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 Papaverine Hydrochloride manufacturer or Papaverine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Papaverine Hydrochloride manufacturer or Papaverine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Papaverine Hydrochloride API Price utilized in the formulation of products. Papaverine Hydrochloride API Price is not always fixed or binding as the Papaverine Hydrochloride Price is obtained through a variety of data sources. The Papaverine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paveron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paveron, including repackagers and relabelers. The FDA regulates Paveron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paveron 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 Paveron manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paveron supplier is an individual or a company that provides Paveron active pharmaceutical ingredient (API) or Paveron finished formulations upon request. The Paveron suppliers may include Paveron API manufacturers, exporters, distributors and traders.
click here to find a list of Paveron 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 Paveron Drug Master File in Japan (Paveron JDMF) empowers Paveron 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 Paveron JDMF during the approval evaluation for pharmaceutical products. At the time of Paveron 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 Paveron suppliers with JDMF on PharmaCompass.
