01 1Osaka Synthetic Organic Chemical Research Institute, Inc.
01 1Japan Pharmaceutical Codex tramazoline hydrochloride salt production dedicated
01 1Japan
Japanese Pharmacopoeia Non-Drug Standard Tramazoline Hydrochloride For manufacturing only
Registration Number : 220MF10207
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2008-09-29
Latest Date of Registration : 2008-09-29
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PharmaCompass offers a list of Tramazoline Hydrochloride Monohydrate 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 Tramazoline Hydrochloride Monohydrate manufacturer or Tramazoline Hydrochloride Monohydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tramazoline Hydrochloride Monohydrate manufacturer or Tramazoline Hydrochloride Monohydrate supplier.
PharmaCompass also assists you with knowing the Tramazoline Hydrochloride Monohydrate API Price utilized in the formulation of products. Tramazoline Hydrochloride Monohydrate API Price is not always fixed or binding as the Tramazoline Hydrochloride Monohydrate Price is obtained through a variety of data sources. The Tramazoline Hydrochloride Monohydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 74195-73-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 74195-73-6, including repackagers and relabelers. The FDA regulates 74195-73-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 74195-73-6 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 74195-73-6 supplier is an individual or a company that provides 74195-73-6 active pharmaceutical ingredient (API) or 74195-73-6 finished formulations upon request. The 74195-73-6 suppliers may include 74195-73-6 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 74195-73-6 Drug Master File in Japan (74195-73-6 JDMF) empowers 74195-73-6 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 74195-73-6 JDMF during the approval evaluation for pharmaceutical products. At the time of 74195-73-6 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 74195-73-6 suppliers with JDMF on PharmaCompass.
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