01 1Katsura Chemical Co., Ltd.
02 1Shiratori Pharmaceutical Co., Ltd.
03 1Siegfried PharmaChemikalien Minden GmbH
01 1Dobutamine hydrochloride
02 1Hydrochloric acid dobutamine Dobutamine Hydrochloride
03 1Japanese Pharmacopoeia hydrochloric acid dobutamine production dedicated
01 2Japan
02 1Switzerland
Registration Number : 219MF10239
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
Japanese Pharmacopoeia Dobutamine Hydrochloride For manufacturing only
Registration Number : 217MF10318
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2005-07-14
Latest Date of Registration : 2006-10-06
Registration Number : 217MF10990
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2007-01-17
A Dobutamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dobutamine Hydrochloride, including repackagers and relabelers. The FDA regulates Dobutamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dobutamine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Dobutamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dobutamine Hydrochloride supplier is an individual or a company that provides Dobutamine Hydrochloride active pharmaceutical ingredient (API) or Dobutamine Hydrochloride finished formulations upon request. The Dobutamine Hydrochloride suppliers may include Dobutamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dobutamine Hydrochloride 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 Dobutamine Hydrochloride Drug Master File in Japan (Dobutamine Hydrochloride JDMF) empowers Dobutamine Hydrochloride 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 Dobutamine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Dobutamine Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Dobutamine Hydrochloride suppliers with JDMF on PharmaCompass.
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