01 1Shiratori Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia hydrochloric acid noscapine production dedicated
01 1Japan
Japanese Pharmacopoeia Noscapine Hydrochloride (for manufacturing purposes only)
Registration Number : 217MF10316
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2005-07-14
Latest Date of Registration : 2009-10-29
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PharmaCompass offers a list of Noscapine 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 Noscapine Hydrochloride manufacturer or Noscapine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Noscapine Hydrochloride manufacturer or Noscapine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Noscapine Hydrochloride API Price utilized in the formulation of products. Noscapine Hydrochloride API Price is not always fixed or binding as the Noscapine Hydrochloride Price is obtained through a variety of data sources. The Noscapine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0963 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0963, including repackagers and relabelers. The FDA regulates N0963 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0963 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 N0963 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0963 supplier is an individual or a company that provides N0963 active pharmaceutical ingredient (API) or N0963 finished formulations upon request. The N0963 suppliers may include N0963 API manufacturers, exporters, distributors and traders.
click here to find a list of N0963 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 N0963 Drug Master File in Japan (N0963 JDMF) empowers N0963 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 N0963 JDMF during the approval evaluation for pharmaceutical products. At the time of N0963 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 N0963 suppliers with JDMF on PharmaCompass.
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