01 2Alps Pharmaceutical Co., Ltd.
01 2Japanese Pharmacopoeia pentoxyverine citrate
01 2Japan
Japanese Pharmacopoeia Pentoxyverine Citrate
Registration Number : 221MF10228
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2009-10-19
Latest Date of Registration : 2009-10-19
Japanese Pharmacopoeia Pentoxyverine Citrate
Registration Number : 225MF10025
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2016-05-06
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PharmaCompass offers a list of Pentoxiverine citrate 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 Pentoxiverine citrate manufacturer or Pentoxiverine citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentoxiverine citrate manufacturer or Pentoxiverine citrate supplier.
PharmaCompass also assists you with knowing the Pentoxiverine citrate API Price utilized in the formulation of products. Pentoxiverine citrate API Price is not always fixed or binding as the Pentoxiverine citrate Price is obtained through a variety of data sources. The Pentoxiverine citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Toclase manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Toclase, including repackagers and relabelers. The FDA regulates Toclase manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Toclase 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 Toclase manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Toclase supplier is an individual or a company that provides Toclase active pharmaceutical ingredient (API) or Toclase finished formulations upon request. The Toclase suppliers may include Toclase API manufacturers, exporters, distributors and traders.
click here to find a list of Toclase 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 Toclase Drug Master File in Japan (Toclase JDMF) empowers Toclase 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 Toclase JDMF during the approval evaluation for pharmaceutical products. At the time of Toclase 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 Toclase suppliers with JDMF on PharmaCompass.
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