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01 1Daito Co., Ltd.
02 2Sanyo Chemical Research Institute Co., Ltd.
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01 3Nicardipine hydrochloride
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01 2Gabon
02 1Japan
Japanese Pharmacopoeia Nicardipine Hydrochloride (for manufacturing only)
Registration Number : 218MF11014
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2006-12-18
Registration Number : 224MF10022
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2012-02-01
Latest Date of Registration : 2012-02-01
Registration Number : 219MF10079
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
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PharmaCompass also assists you with knowing the Nicardipine Hydrochloride API Price utilized in the formulation of products. Nicardipine Hydrochloride API Price is not always fixed or binding as the Nicardipine Hydrochloride Price is obtained through a variety of data sources. The Nicardipine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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A Cardene In 4.8% Dextrose In Plastic Container supplier is an individual or a company that provides Cardene In 4.8% Dextrose In Plastic Container active pharmaceutical ingredient (API) or Cardene In 4.8% Dextrose In Plastic Container finished formulations upon request. The Cardene In 4.8% Dextrose In Plastic Container suppliers may include Cardene In 4.8% Dextrose In Plastic Container 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 Cardene In 4.8% Dextrose In Plastic Container Drug Master File in Japan (Cardene In 4.8% Dextrose In Plastic Container JDMF) empowers Cardene In 4.8% Dextrose In Plastic Container 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 Cardene In 4.8% Dextrose In Plastic Container JDMF during the approval evaluation for pharmaceutical products. At the time of Cardene In 4.8% Dextrose In Plastic Container 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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