01 1Curia Spain S. A. U.
02 1Dojin Pharmaceutical Chemical Co., Ltd.
03 1FORMOSA LABORATORIES, INC.
04 1MSD International GmbH (Singapore Branch)
05 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
01 1Betamethasone
02 1Betamethasone "Teva"
03 1Betamethasone Butyrate Propionicate micronized
04 1Betamethasone butyrate propionate
05 1Betamethasone butyric acid ester propionic acid ester
01 1Italy
02 1Japan
03 1Singapore
04 1Taiwan
05 1U.S.A
Betamethasone Butyrate Propionate micronized
Registration Number : 231MF10083
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2019-04-05
Latest Date of Registration : 2019-04-05
Betamethasone butyrate propionate "Dozin"
Registration Number : 217MF10386
Registrant's Address : 8-1 Higashinakagawara, Segami-cho, Fukushima City, Fukushima Prefecture
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2024-08-22
Betamethasone butyrate propionate
Registration Number : 229MF10177
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2017-09-07
Latest Date of Registration : 2021-08-20
Registration Number : 224MF10129
Registrant's Address : 50 Tuas West Drive Singapore 638408
Initial Date of Registration : 2012-07-19
Latest Date of Registration : 2012-07-19
Registration Number : 218MF10625
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2006-07-20
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A Betamethasonvalerat Mikron manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betamethasonvalerat Mikron, including repackagers and relabelers. The FDA regulates Betamethasonvalerat Mikron manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betamethasonvalerat Mikron API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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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 Betamethasonvalerat Mikron Drug Master File in Japan (Betamethasonvalerat Mikron JDMF) empowers Betamethasonvalerat Mikron 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 Betamethasonvalerat Mikron JDMF during the approval evaluation for pharmaceutical products. At the time of Betamethasonvalerat Mikron JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 5 companies offering Betamethasonvalerat Mikron
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