01 1AMSA S. p. A.
01 1METOCLOPRAMIDE DIHYDROCHLORIDE
01 1Italy
METOCLOPRAMIDE DIHYDROCHLORIDE
Registration Number : 221MF10057
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2009-03-19
Latest Date of Registration : 2024-12-18
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PharmaCompass offers a list of Metoclopramide 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 Metoclopramide Hydrochloride manufacturer or Metoclopramide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metoclopramide Hydrochloride manufacturer or Metoclopramide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Metoclopramide Hydrochloride API Price utilized in the formulation of products. Metoclopramide Hydrochloride API Price is not always fixed or binding as the Metoclopramide Hydrochloride Price is obtained through a variety of data sources. The Metoclopramide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metozolv ODT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metozolv ODT, including repackagers and relabelers. The FDA regulates Metozolv ODT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metozolv ODT 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 Metozolv ODT supplier is an individual or a company that provides Metozolv ODT active pharmaceutical ingredient (API) or Metozolv ODT finished formulations upon request. The Metozolv ODT suppliers may include Metozolv ODT API manufacturers, exporters, distributors and traders.
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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 Metozolv ODT Drug Master File in Japan (Metozolv ODT JDMF) empowers Metozolv ODT 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 Metozolv ODT JDMF during the approval evaluation for pharmaceutical products. At the time of Metozolv ODT 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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