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 NCGC00024440-03 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024440-03, including repackagers and relabelers. The FDA regulates NCGC00024440-03 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024440-03 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 NCGC00024440-03 supplier is an individual or a company that provides NCGC00024440-03 active pharmaceutical ingredient (API) or NCGC00024440-03 finished formulations upon request. The NCGC00024440-03 suppliers may include NCGC00024440-03 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 NCGC00024440-03 Drug Master File in Japan (NCGC00024440-03 JDMF) empowers NCGC00024440-03 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 NCGC00024440-03 JDMF during the approval evaluation for pharmaceutical products. At the time of NCGC00024440-03 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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