01 10Yashiro Pharmaceutical Co., Ltd.
01 1Barbital
02 2Phenobarbital P
03 2Phenobarbital PPT
04 2Phenobarbital PPT55
05 2Phenobarbital S
06 1Phenobarbital SS
01 10Blank
Registration Number : 218MF10253
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-17
Registration Number : 218MF10252
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-16
Registration Number : 218MF10251
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-16
Registration Number : 218MF10250
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-16
Registration Number : 218MF10249
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-16
Registration Number : 225MF10078
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2013-04-18
Registration Number : 225MF10077
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2013-04-18
Registration Number : 225MF10076
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2013-04-18
Registration Number : 225MF10075
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2013-04-18
Registration Number : 225MF10074
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2013-04-18
Latest Date of Registration : 2013-04-18
47
PharmaCompass offers a list of Phenobarbital API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Phenobarbital manufacturer or Phenobarbital supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenobarbital manufacturer or Phenobarbital supplier.
A Blu-phen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Blu-phen, including repackagers and relabelers. The FDA regulates Blu-phen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Blu-phen 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 Blu-phen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Blu-phen supplier is an individual or a company that provides Blu-phen active pharmaceutical ingredient (API) or Blu-phen finished formulations upon request. The Blu-phen suppliers may include Blu-phen API manufacturers, exporters, distributors and traders.
click here to find a list of Blu-phen suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Blu-phen Drug Master File in Japan (Blu-phen JDMF) empowers Blu-phen 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 Blu-phen JDMF during the approval evaluation for pharmaceutical products. At the time of Blu-phen 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 Blu-phen suppliers with JDMF on PharmaCompass.
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