01 1AMSA S. p. A.
02 1Ipca Laboratories Limited
03 1Joko Pharmaceutical Co., Ltd.
04 1Kongo Chemical Co., Ltd.
05 1Liaoyuan Silver Eagle Pharmaceutical Co. , Ltd.
01 1METOCLOPRAMIDE
02 4Metoclopramide
01 1China
02 1India
03 1Italy
04 1Japan
05 1Blank
Registration Number : 305MF10087
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2023-07-19
Latest Date of Registration : 2024-06-12
Registration Number : 220MF10231
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2008-11-17
Latest Date of Registration : 2008-11-17
Registration Number : 220MF10256
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2008-12-12
Latest Date of Registration : 2008-12-12
Registration Number : 305MF10123
Registrant's Address : No. 2 Wealth Northern Road, Youyi Industry Area of Liaoyuan Economic Developmen...
Initial Date of Registration : 2023-11-29
Latest Date of Registration : 2023-11-29
Registration Number : 306MF10073
Registrant's Address : 5 Kajiga Isshiki Nishi 1-chome, Kitanagoya City, Aichi Prefecture
Initial Date of Registration : 2024-05-29
Latest Date of Registration : 2024-05-29
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PharmaCompass offers a list of Metoclopramide 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 manufacturer or Metoclopramide supplier for your needs.
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A Reliveran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reliveran, including repackagers and relabelers. The FDA regulates Reliveran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reliveran 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 Reliveran supplier is an individual or a company that provides Reliveran active pharmaceutical ingredient (API) or Reliveran finished formulations upon request. The Reliveran suppliers may include Reliveran 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 Reliveran Drug Master File in Japan (Reliveran JDMF) empowers Reliveran 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 Reliveran JDMF during the approval evaluation for pharmaceutical products. At the time of Reliveran 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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