01 1Chongqing Shenghuaxi Pharmaceutical Co. ,Ltd
02 1Daito Co., Ltd.
03 2ILDONG PHARMACEUTICAL CO. , LTD.
04 1Kyowa Pharma Chemical Co., Ltd.
05 1Lusochimica S. p. A.
06 1Permakem Asia Co., Ltd.
07 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
08 2Sanyo Chemical Research Institute Co., Ltd.
01 1Benidipine HCl
02 1Benidipine Hydrochloride
03 5Benidipine hydrochloride
04 1Day stations benidipine hydrochloride (production only)
05 1Japanese Pharmacopoeia benidipine hydrochloride "production-only"
06 1Japanese Pharmacopoeia benidipine hydrochloride (production only)
01 1China
02 2Gabon
03 2Italy
04 3Japan
05 2South Korea
Registration Number : 225MF10065
Registrant's Address : No. 8 Jiangqiao Road, Nan an District Chongqing China
Initial Date of Registration : 2013-03-27
Latest Date of Registration : 2013-03-27
JP Benidipine Hydrochloride (for manufacturing only)
Registration Number : 218MF11034
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2010-01-07
Registration Number : 218MF10739
Registrant's Address : 2. Baumoe-ro 27-gil, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2006-09-06
Registration Number : 304MF10084
Registrant's Address : 2. Baumoe-ro 27-gil, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2022-06-01
Latest Date of Registration : 2022-06-01
Japanese Pharmacopoeia Benidipine Hydrochloride (for manufacturing only)
Registration Number : 225MF10209
Registrant's Address : 530 Chokeiji, Takaoka City, Toyama Prefecture
Initial Date of Registration : 2013-11-14
Latest Date of Registration : 2013-11-14
Registration Number : 227MF10092
Registrant's Address : Via Libornese, 897 56122 La Vettola, Pisa
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Registration Number : 229MF10203
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2017-11-21
Latest Date of Registration : 2017-11-21
Registration Number : 219MF10171
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2007-05-24
Latest Date of Registration : 2007-05-24
Registration Number : 223MF10180
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2011-12-27
Japanese Pharmacopoeia Benidipine Hydrochloride "For manufacturing only"
Registration Number : 218MF10731
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2007-01-10
A Benidipine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benidipine Hydrochloride, including repackagers and relabelers. The FDA regulates Benidipine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benidipine 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 Benidipine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benidipine Hydrochloride supplier is an individual or a company that provides Benidipine Hydrochloride active pharmaceutical ingredient (API) or Benidipine Hydrochloride finished formulations upon request. The Benidipine Hydrochloride suppliers may include Benidipine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Benidipine 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 Benidipine Hydrochloride Drug Master File in Japan (Benidipine Hydrochloride JDMF) empowers Benidipine 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 Benidipine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Benidipine 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 Benidipine Hydrochloride suppliers with JDMF on PharmaCompass.
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