01 1Alps Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia funnel extract
01 1Japan
Japanese Pharmacopoeia Belladonna Extract
Registration Number : 217MF11030
Registrant's Address : 10-50, Mukai-cho 2-chome, Furukawa-cho, Hida City, Gifu Prefecture
Initial Date of Registration : 2005-12-02
Latest Date of Registration : 2010-04-01
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PharmaCompass offers a list of Hyoscyamine Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Hyoscyamine Sulfate manufacturer or Hyoscyamine Sulfate supplier for your needs.
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A Hyoscyamine Sulphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyoscyamine Sulphate, including repackagers and relabelers. The FDA regulates Hyoscyamine Sulphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyoscyamine Sulphate 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 Hyoscyamine Sulphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hyoscyamine Sulphate supplier is an individual or a company that provides Hyoscyamine Sulphate active pharmaceutical ingredient (API) or Hyoscyamine Sulphate finished formulations upon request. The Hyoscyamine Sulphate suppliers may include Hyoscyamine Sulphate API manufacturers, exporters, distributors and traders.
click here to find a list of Hyoscyamine Sulphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Hyoscyamine Sulphate Drug Master File in Japan (Hyoscyamine Sulphate JDMF) empowers Hyoscyamine Sulphate 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 Hyoscyamine Sulphate JDMF during the approval evaluation for pharmaceutical products. At the time of Hyoscyamine Sulphate 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 Hyoscyamine Sulphate suppliers with JDMF on PharmaCompass.
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