01 2Yashiro Pharmaceutical Co., Ltd.
01 2Phenobarbital sodium (Yashiro)
01 2Blank
Phenobarbital Sodium (Yatsushiro)
Registration Number : 227MF10203
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2015-08-10
Latest Date of Registration : 2015-08-10
Phenobarbital Sodium (Yatsushiro)
Registration Number : 218MF10254
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-25
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PharmaCompass offers a list of Phenobarbital Sodium 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 Phenobarbital Sodium manufacturer or Phenobarbital Sodium supplier for your needs.
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A Fenobarbital natrium [Polish] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fenobarbital natrium [Polish], including repackagers and relabelers. The FDA regulates Fenobarbital natrium [Polish] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fenobarbital natrium [Polish] 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 Fenobarbital natrium [Polish] supplier is an individual or a company that provides Fenobarbital natrium [Polish] active pharmaceutical ingredient (API) or Fenobarbital natrium [Polish] finished formulations upon request. The Fenobarbital natrium [Polish] suppliers may include Fenobarbital natrium [Polish] 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 Fenobarbital natrium [Polish] Drug Master File in Japan (Fenobarbital natrium [Polish] JDMF) empowers Fenobarbital natrium [Polish] 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 Fenobarbital natrium [Polish] JDMF during the approval evaluation for pharmaceutical products. At the time of Fenobarbital natrium [Polish] 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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