01 1Curia Spain S. A. U.
02 1HOVIONE FARMACIENCIA SA
03 1Newchem S. p. A.
01 1Betamethasone ester sodium
02 1Betamethasone sodium phosphate
03 1Day stations betamethasone acid ester sodium
01 1Italy
02 1Portugal
03 1U.S.A
JP Betamethasone Sodium Phosphate
Registration Number : 219MF10235
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
Betamethasone sodium phosphate
Registration Number : 220MF10125
Registrant's Address : Sete Casas 2674-506 Loures PORTUGAL
Initial Date of Registration : 2008-05-15
Latest Date of Registration : 2022-07-27
Betamethasone sodium phosphate
Registration Number : 217MF10601
Registrant's Address : Via San Vittore, 39 - 20123 Milano (Italy)
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2024-12-25
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PharmaCompass offers a list of Betamethasone Sodium Phosphate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Betamethasone Sodium Phosphate manufacturer or Betamethasone Sodium Phosphate supplier for your needs.
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A Betavet Soluspan (Veterinary) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betavet Soluspan (Veterinary), including repackagers and relabelers. The FDA regulates Betavet Soluspan (Veterinary) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betavet Soluspan (Veterinary) 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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A Betavet Soluspan (Veterinary) supplier is an individual or a company that provides Betavet Soluspan (Veterinary) active pharmaceutical ingredient (API) or Betavet Soluspan (Veterinary) finished formulations upon request. The Betavet Soluspan (Veterinary) suppliers may include Betavet Soluspan (Veterinary) API manufacturers, exporters, distributors and traders.
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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 Betavet Soluspan (Veterinary) Drug Master File in Japan (Betavet Soluspan (Veterinary) JDMF) empowers Betavet Soluspan (Veterinary) 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 Betavet Soluspan (Veterinary) JDMF during the approval evaluation for pharmaceutical products. At the time of Betavet Soluspan (Veterinary) 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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