01 1Alps Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Butoropiumu bromide
01 1Japan
Japanese Pharmacopoeia Butropium Bromide
Registration Number : 221MF10173
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2009-07-30
Latest Date of Registration : 2009-07-30
A Tiotropium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiotropium Bromide, including repackagers and relabelers. The FDA regulates Tiotropium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiotropium Bromide 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 Tiotropium Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiotropium Bromide supplier is an individual or a company that provides Tiotropium Bromide active pharmaceutical ingredient (API) or Tiotropium Bromide finished formulations upon request. The Tiotropium Bromide suppliers may include Tiotropium Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Tiotropium Bromide 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 Tiotropium Bromide Drug Master File in Japan (Tiotropium Bromide JDMF) empowers Tiotropium Bromide 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 Tiotropium Bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Tiotropium Bromide 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 Tiotropium Bromide suppliers with JDMF on PharmaCompass.
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