01 1Ajinomoto Co., Inc.
02 1Kyowa Hakko Bio Co., Ltd.
01 2Japanese Pharmacopoeia L- arginine hydrochloride (production only)
01 2Japan
Japanese Pharmacopoeia L-Arginine Hydrochloride (for manufacturing only)
Registration Number : 218MF10637
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2006-07-20
Japanese Pharmacopoeia L-Arginine Hydrochloride (for manufacturing only)
Registration Number : 219MF10190
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-06-08
Latest Date of Registration : 2007-06-08
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PharmaCompass offers a list of L-Arginine Hydrochloride API 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 L-Arginine Hydrochloride API manufacturer or L-Arginine Hydrochloride API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Arginine Hydrochloride API manufacturer or L-Arginine Hydrochloride API supplier.
PharmaCompass also assists you with knowing the L-Arginine Hydrochloride API API Price utilized in the formulation of products. L-Arginine Hydrochloride API API Price is not always fixed or binding as the L-Arginine Hydrochloride API Price is obtained through a variety of data sources. The L-Arginine Hydrochloride API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A R-gene 10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of R-gene 10, including repackagers and relabelers. The FDA regulates R-gene 10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. R-gene 10 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A R-gene 10 supplier is an individual or a company that provides R-gene 10 active pharmaceutical ingredient (API) or R-gene 10 finished formulations upon request. The R-gene 10 suppliers may include R-gene 10 API manufacturers, exporters, distributors and traders.
click here to find a list of R-gene 10 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 R-gene 10 Drug Master File in Japan (R-gene 10 JDMF) empowers R-gene 10 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 R-gene 10 JDMF during the approval evaluation for pharmaceutical products. At the time of R-gene 10 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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