01 2Katsura Chemical Co., Ltd.
01 1Atropine Sulfate Hydrate-K
02 1Atropine sulfate hydrate
01 2Japan
Registration Number : 221MF10005
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2009-01-13
Latest Date of Registration : 2009-01-13
Registration Number : 303MF10180
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2021-12-15
Latest Date of Registration : 2021-12-15
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PharmaCompass offers a list of Atropine Sulfate 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 Atropine Sulfate manufacturer or Atropine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atropine Sulfate manufacturer or Atropine Sulfate supplier.
PharmaCompass also assists you with knowing the Atropine Sulfate API Price utilized in the formulation of products. Atropine Sulfate API Price is not always fixed or binding as the Atropine Sulfate Price is obtained through a variety of data sources. The Atropine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AtroPen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AtroPen, including repackagers and relabelers. The FDA regulates AtroPen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AtroPen 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 AtroPen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AtroPen supplier is an individual or a company that provides AtroPen active pharmaceutical ingredient (API) or AtroPen finished formulations upon request. The AtroPen suppliers may include AtroPen API manufacturers, exporters, distributors and traders.
click here to find a list of AtroPen 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 AtroPen Drug Master File in Japan (AtroPen JDMF) empowers AtroPen 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 AtroPen JDMF during the approval evaluation for pharmaceutical products. At the time of AtroPen 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 AtroPen suppliers with JDMF on PharmaCompass.
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