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.
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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 H754 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of H754, including repackagers and relabelers. The FDA regulates H754 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. H754 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 H754 supplier is an individual or a company that provides H754 active pharmaceutical ingredient (API) or H754 finished formulations upon request. The H754 suppliers may include H754 API manufacturers, exporters, distributors and traders.
click here to find a list of H754 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 H754 Drug Master File in Japan (H754 JDMF) empowers H754 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 H754 JDMF during the approval evaluation for pharmaceutical products. At the time of H754 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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