Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1Zhejiang Hengkang Pharmaceutical Co. , Ltd.
02 1Daiwa Pharmaceutical Industries Co., Ltd.
03 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
04 1Siegfried Evionnaz SA
05 1Zhejiang Liaoyuan Pharmaceutical Co. , Ltd.
06 1Zhejiang Sanmen Kangning Chemical Co. ,Ltd
01 1Day stations ticlopidine hydrochloride (production only)
02 1Japanese Pharmacopoeia ticlopidine hydrochloride (production only)
03 1Ticlopidine Hydrochloride
04 1Ticlopidine Hydrochloride JP
05 1Ticlopidine hydrochloride
06 1Ticlopidine hydrochloride "Teva"
01 3China
02 1Italy
03 1Japan
04 1Switzerland
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registration Number : 223MF10137
Registrant's Address : No. 1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China
Initial Date of Registration : 2011-08-19
Latest Date of Registration : 2011-08-19
Japanese Pharmacopoeia Ticlopidine Hydrochloride (for manufacturing only)
Registration Number : 219MF10156
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2011-09-28
Ticlopidine hydrochloride (Teva)
Registration Number : 219MF10159
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2007-05-15
Latest Date of Registration : 2007-05-15
Registration Number : 219MF10303
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2007-09-28
Latest Date of Registration : 2018-11-14
JP Ticlopidine Hydrochloride (for manufacturing only)
Registration Number : 219MF10251
Registrant's Address : Zhejiang Provincial Chemical and Medical Raw Material Base Linhai Zone Duqiao town, L...
Initial Date of Registration : 2007-07-26
Latest Date of Registration : 2019-03-15
Registration Number : 222MF10127
Registrant's Address : Jia'ao Guishan, Sanmen County, Zhejiang, China
Initial Date of Registration : 2010-04-12
Latest Date of Registration : 2010-04-12
A Ticlopidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ticlopidine Hydrochloride, including repackagers and relabelers. The FDA regulates Ticlopidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ticlopidine 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 Ticlopidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ticlopidine Hydrochloride supplier is an individual or a company that provides Ticlopidine Hydrochloride active pharmaceutical ingredient (API) or Ticlopidine Hydrochloride finished formulations upon request. The Ticlopidine Hydrochloride suppliers may include Ticlopidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ticlopidine 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 Ticlopidine Hydrochloride Drug Master File in Japan (Ticlopidine Hydrochloride JDMF) empowers Ticlopidine 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 Ticlopidine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Ticlopidine 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 Ticlopidine Hydrochloride suppliers with JDMF on PharmaCompass.
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