01 1Daito Co., Ltd.
02 1Katsura Chemical Co., Ltd.
03 1Kyowa Pharma Chemical Co., Ltd.
04 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
05 1Siegfried PharmaChemikalien Minden GmbH
01 1Day stations dopamine hydrochloride (production only)
02 1Dopamine Hydrochloride
03 2Dopamine hydrochloride
04 1Japanese Pharmacopoeia dopamine hydrochloride (production only)
01 1Italy
02 3Japan
03 1Switzerland
JP Dopamine Hydrochloride (for manufacturing only)
Registration Number : 218MF10917
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
Registration Number : 218MF10897
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
Japanese Pharmacopoeia Dopamine Hydrochloride (for manufacturing only)
Registration Number : 222MF10235
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2010-09-30
Latest Date of Registration : 2016-12-05
Registration Number : 304MF10111
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2022-08-03
Latest Date of Registration : 2022-08-03
Registration Number : 218MF10519
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2006-05-18
Latest Date of Registration : 2006-05-18
A CAS-62-31-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-62-31-7, including repackagers and relabelers. The FDA regulates CAS-62-31-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-62-31-7 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 CAS-62-31-7 supplier is an individual or a company that provides CAS-62-31-7 active pharmaceutical ingredient (API) or CAS-62-31-7 finished formulations upon request. The CAS-62-31-7 suppliers may include CAS-62-31-7 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-62-31-7 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 CAS-62-31-7 Drug Master File in Japan (CAS-62-31-7 JDMF) empowers CAS-62-31-7 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 CAS-62-31-7 JDMF during the approval evaluation for pharmaceutical products. At the time of CAS-62-31-7 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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