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