01 1Midori Chemical Co., Ltd.
01 1Japanese Pharmacopoeia hydrochloric acid tolperisone
01 1Japan
Tolperisone Hydrochloride, Japanese Pharmacopoeia
Registration Number : 217MF10876
Registrant's Address : 3-19-12 Kamiochiai, Shinjuku-ku, Tokyo
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2006-07-03
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PharmaCompass offers a list of Tolperisone 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 Tolperisone manufacturer or Tolperisone supplier for your needs.
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PharmaCompass also assists you with knowing the Tolperisone API Price utilized in the formulation of products. Tolperisone API Price is not always fixed or binding as the Tolperisone Price is obtained through a variety of data sources. The Tolperisone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Abbsa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Abbsa, including repackagers and relabelers. The FDA regulates Abbsa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Abbsa 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 Abbsa supplier is an individual or a company that provides Abbsa active pharmaceutical ingredient (API) or Abbsa finished formulations upon request. The Abbsa suppliers may include Abbsa 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 Abbsa Drug Master File in Japan (Abbsa JDMF) empowers Abbsa 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 Abbsa JDMF during the approval evaluation for pharmaceutical products. At the time of Abbsa 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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