01 1Daito Co., Ltd.
02 2IcromS. p. A.
03 2Permachem Asia Co., Ltd.
01 1Hydrochloric acid tiapride
02 1Outsiders regulations hydrochloric acid tiapride (production only)
03 3Tiapride hydrochloride
01 2Italy
02 3Japan
Registration Number : 222MF10276
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2010-12-17
Latest Date of Registration : 2010-12-17
Registration Number : 227MF10074
Registrant's Address : Via Delle Arti 33, 20863 Concorezzo (MB), Italy
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Off-label use thiapride hydrochloride (for manufacturing purposes only)
Registration Number : 218MF10085
Registrant's Address : Via Delle Arti 33, 20049 Concorezzo (MI), Italy
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2010-04-05
Registration Number : 217MF10714
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2010-03-09
Registration Number : 226MF10077
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2014-04-02
Latest Date of Registration : 2014-04-02
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PharmaCompass offers a list of Tiapride Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tiapride Hydrochloride manufacturer or Tiapride Hydrochloride supplier for your needs.
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A Tiapride Sanofi-Synthelabo Brand manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiapride Sanofi-Synthelabo Brand, including repackagers and relabelers. The FDA regulates Tiapride Sanofi-Synthelabo Brand manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiapride Sanofi-Synthelabo Brand 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 Tiapride Sanofi-Synthelabo Brand manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tiapride Sanofi-Synthelabo Brand supplier is an individual or a company that provides Tiapride Sanofi-Synthelabo Brand active pharmaceutical ingredient (API) or Tiapride Sanofi-Synthelabo Brand finished formulations upon request. The Tiapride Sanofi-Synthelabo Brand suppliers may include Tiapride Sanofi-Synthelabo Brand API manufacturers, exporters, distributors and traders.
click here to find a list of Tiapride Sanofi-Synthelabo Brand suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Tiapride Sanofi-Synthelabo Brand Drug Master File in Japan (Tiapride Sanofi-Synthelabo Brand JDMF) empowers Tiapride Sanofi-Synthelabo Brand 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 Tiapride Sanofi-Synthelabo Brand JDMF during the approval evaluation for pharmaceutical products. At the time of Tiapride Sanofi-Synthelabo Brand 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 Tiapride Sanofi-Synthelabo Brand suppliers with JDMF on PharmaCompass.
We have 3 companies offering Tiapride Sanofi-Synthelabo Brand
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