01 1Shanghai Wonder Pharmaceutical Co. , Ltd.
02 1Siegfried PharmaChemikalien Minden GmbH
01 1Diprophylline Diprophylline
02 1Japan Pharmaceutical Codex diprophylline (production only)
01 1China
02 1Switzerland
Japanese Pharmacopoeia Non-Drug Standard Diprophylline (For manufacturing only)
Registration Number : 226MF10197
Registrant's Address : No. 2068, Jinzhang Road, Jinshan Area, Shanghai, P. R. China
Initial Date of Registration : 2014-10-27
Latest Date of Registration : 2014-10-27
Registration Number : 217MF10982
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2010-02-25
A Nsc241225 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nsc241225, including repackagers and relabelers. The FDA regulates Nsc241225 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nsc241225 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Nsc241225 supplier is an individual or a company that provides Nsc241225 active pharmaceutical ingredient (API) or Nsc241225 finished formulations upon request. The Nsc241225 suppliers may include Nsc241225 API manufacturers, exporters, distributors and traders.
click here to find a list of Nsc241225 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 Nsc241225 Drug Master File in Japan (Nsc241225 JDMF) empowers Nsc241225 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 Nsc241225 JDMF during the approval evaluation for pharmaceutical products. At the time of Nsc241225 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 Nsc241225 suppliers with JDMF on PharmaCompass.
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