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01 10Yashiro Pharmaceutical Co., Ltd.
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01 1Barbital
02 2Phenobarbital P
03 2Phenobarbital PPT
04 2Phenobarbital PPT55
05 2Phenobarbital S
06 1Phenobarbital SS
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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
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PharmaCompass offers a list of Phenobarbital 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 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.
PharmaCompass also assists you with knowing the Phenobarbital API Price utilized in the formulation of products. Phenobarbital API Price is not always fixed or binding as the Phenobarbital Price is obtained through a variety of data sources. The Phenobarbital Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A barbapil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of barbapil, including repackagers and relabelers. The FDA regulates barbapil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. barbapil 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 barbapil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A barbapil supplier is an individual or a company that provides barbapil active pharmaceutical ingredient (API) or barbapil finished formulations upon request. The barbapil suppliers may include barbapil API manufacturers, exporters, distributors and traders.
click here to find a list of barbapil 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 barbapil Drug Master File in Japan (barbapil JDMF) empowers barbapil 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 barbapil JDMF during the approval evaluation for pharmaceutical products. At the time of barbapil 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 barbapil suppliers with JDMF on PharmaCompass.
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