Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Daito Co., Ltd.
03 1Dijia Pharmaceutical Group Co. , Ltd.
04 1Ipca Laboratories Limited
05 2Permakem Asia Co., Ltd.
06 1Sanyo Chemical Research Institute Co., Ltd.
07 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Day stations nifedipine (production only)
02 1Japanese Pharmacopoeia nifedipine (production only)
03 1NIFEDIPINE
04 4Nifedipine
05 1Nifedipine "Teva / Caronno"
01 1China
02 1Gabon
03 1India
04 1Italy
05 3Japan
06 1Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 219MF10249
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2007-07-26
Latest Date of Registration : 2013-05-10
JP Nifedipine (for manufacturing only)
Registration Number : 217MF10626
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2007-05-02
Registration Number : 227MF10111
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (West), Mumbai 400 067, India
Initial Date of Registration : 2015-04-21
Latest Date of Registration : 2015-04-21
Registration Number : 217MF10703
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2007-06-18
Registration Number : 229MF10181
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2017-09-28
Latest Date of Registration : 2017-09-28
Registration Number : 226MF10110
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2014-05-26
Latest Date of Registration : 2021-11-10
Registration Number : 305MF10006
Registrant's Address : No. 268 Tianrun Road, Wendeng Economic Development Zone, Weihai, Shandong, China
Initial Date of Registration : 2023-01-18
Latest Date of Registration : 2023-01-18
Japanese Pharmacopoeia Nifedipine (for manufacturing only)
Registration Number : 217MF10157
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2008-03-28
A Nifedipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nifedipine, including repackagers and relabelers. The FDA regulates Nifedipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nifedipine 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 Nifedipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nifedipine supplier is an individual or a company that provides Nifedipine active pharmaceutical ingredient (API) or Nifedipine finished formulations upon request. The Nifedipine suppliers may include Nifedipine API manufacturers, exporters, distributors and traders.
click here to find a list of Nifedipine 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 Nifedipine Drug Master File in Japan (Nifedipine JDMF) empowers Nifedipine 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 Nifedipine JDMF during the approval evaluation for pharmaceutical products. At the time of Nifedipine 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 Nifedipine suppliers with JDMF on PharmaCompass.
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