01 1Alps Pharmaceutical Co., Ltd.
02 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
01 1Japanese Pharmacopoeia scopolamine hydrobromide hydrate
02 1Scopolamine hydrobromide hydrate
01 1Germany
02 1Japan
Japanese Pharmacopoeia Scopolamine Hydrobromide Hydrate
Registration Number : 227MF10032
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2015-01-23
Latest Date of Registration : 2015-01-23
Scopolamine hydrobromide hydrate
Registration Number : 221MF10105
Registrant's Address : Binger Strasse 173, 55216 Ingelheim am Rhein
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2009-05-27
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PharmaCompass offers a list of Scopolamine Hydrobromide 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 Scopolamine Hydrobromide manufacturer or Scopolamine Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Scopolamine Hydrobromide API Price utilized in the formulation of products. Scopolamine Hydrobromide API Price is not always fixed or binding as the Scopolamine Hydrobromide Price is obtained through a variety of data sources. The Scopolamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CAS-114-49-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-114-49-8, including repackagers and relabelers. The FDA regulates CAS-114-49-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-114-49-8 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 CAS-114-49-8 supplier is an individual or a company that provides CAS-114-49-8 active pharmaceutical ingredient (API) or CAS-114-49-8 finished formulations upon request. The CAS-114-49-8 suppliers may include CAS-114-49-8 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-114-49-8 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 CAS-114-49-8 Drug Master File in Japan (CAS-114-49-8 JDMF) empowers CAS-114-49-8 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 CAS-114-49-8 JDMF during the approval evaluation for pharmaceutical products. At the time of CAS-114-49-8 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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