01 1Daito Co., Ltd.
01 1Nicardipine hydrochloride
01 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
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PharmaCompass offers a list of Nicardipine Hydrochloride 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 Nicardipine Hydrochloride manufacturer or Nicardipine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nicardipine Hydrochloride manufacturer or Nicardipine Hydrochloride supplier.
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.
A N0635 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0635, including repackagers and relabelers. The FDA regulates N0635 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0635 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 N0635 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0635 supplier is an individual or a company that provides N0635 active pharmaceutical ingredient (API) or N0635 finished formulations upon request. The N0635 suppliers may include N0635 API manufacturers, exporters, distributors and traders.
click here to find a list of N0635 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 N0635 Drug Master File in Japan (N0635 JDMF) empowers N0635 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 N0635 JDMF during the approval evaluation for pharmaceutical products. At the time of N0635 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 N0635 suppliers with JDMF on PharmaCompass.
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