01 1Daito Co., Ltd.
02 2QIDONG DONGYUE PHARMACEUTICAL CO. , LTD.
03 2Yabao Pharmaceutical Group Co. , Ltd.
04 1Yashiro Pharmaceutical Co., Ltd.
01 4Dipyridamole
02 1Japanese Pharmacopoeia dipyridamole
03 1Japanese Pharmacopoeia drugs dipyridamole (production only)
01 4China
02 1India
03 1Blank
Japanese Pharmacopoeia Drug Dipyridamole (for manufacturing only)
Registration Number : 219MF10223
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2011-02-10
Japanese Pharmacopoeia Dipyridamole
Registration Number : 222MF10071
Registrant's Address : No. 268 SHANGHAI RD. BINJIANG FINE CHEMICAL INDUSTRY ZONE, QIDONG CITY, JIANGSU PROVI...
Initial Date of Registration : 2010-02-25
Latest Date of Registration : 2016-04-20
Registration Number : 221MF10089
Registrant's Address : HEHE TOWN, QIDONG CITY, JIANGSU PROVINCE, CHINA
Initial Date of Registration : 2009-05-13
Latest Date of Registration : 2009-05-13
Registration Number : 227MF10161
Registrant's Address : No. 43, Fuminlu, Ruicheng, Shanxi, P. R. China
Initial Date of Registration : 2015-06-18
Latest Date of Registration : 2015-06-18
Registration Number : 218MF10665
Registrant's Address : No. 43, Fuminlu, Ruicheng, Shanxi, P. R. China
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2011-01-26
Registration Number : 218MF10244
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2016-05-13
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PharmaCompass offers a list of Dipyridamole 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 Dipyridamole manufacturer or Dipyridamole supplier for your needs.
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A Prestwick3_000142 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000142, including repackagers and relabelers. The FDA regulates Prestwick3_000142 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000142 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 Prestwick3_000142 supplier is an individual or a company that provides Prestwick3_000142 active pharmaceutical ingredient (API) or Prestwick3_000142 finished formulations upon request. The Prestwick3_000142 suppliers may include Prestwick3_000142 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 Prestwick3_000142 Drug Master File in Japan (Prestwick3_000142 JDMF) empowers Prestwick3_000142 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 Prestwick3_000142 JDMF during the approval evaluation for pharmaceutical products. At the time of Prestwick3_000142 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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