01 1Daito Co., Ltd.
02 2IcromS. p. A.
03 2Permakem 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
Tiapride hydrochloride (for manufacturing 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 : 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
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
A Tiapride Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiapride Hydrochloride, including repackagers and relabelers. The FDA regulates Tiapride Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiapride 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 Tiapride Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiapride Hydrochloride supplier is an individual or a company that provides Tiapride Hydrochloride active pharmaceutical ingredient (API) or Tiapride Hydrochloride finished formulations upon request. The Tiapride Hydrochloride suppliers may include Tiapride Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tiapride 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 Tiapride Hydrochloride Drug Master File in Japan (Tiapride Hydrochloride JDMF) empowers Tiapride 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 Tiapride Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Tiapride 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 Tiapride Hydrochloride suppliers with JDMF on PharmaCompass.
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