01 1Xellia (Taizhou) Pharmaceuticals Co. ,Ltd
02 1Xellia Pharmaceuticals AS
01 2Japanese Pharmacopoeia bacitracin
01 2Denmark
Japanese Pharmacopoeia Bacitracin
Registration Number : 218MF10935
Registrant's Address : Harbitzalle(´)en 3, P. O. Box 158 Skφyen N-0212 Oslo, Norway
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
Japanese Pharmacopoeia Bacitracin
Registration Number : 225MF10193
Registrant's Address : 108 Binhai Road, Taizhou, Zhejiang 318000 PRC, China
Initial Date of Registration : 2013-10-09
Latest Date of Registration : 2013-10-09
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PharmaCompass also assists you with knowing the Bacitracin Zinc API Price utilized in the formulation of products. Bacitracin Zinc API Price is not always fixed or binding as the Bacitracin Zinc Price is obtained through a variety of data sources. The Bacitracin Zinc Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Baciguent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Baciguent, including repackagers and relabelers. The FDA regulates Baciguent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Baciguent 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 Baciguent supplier is an individual or a company that provides Baciguent active pharmaceutical ingredient (API) or Baciguent finished formulations upon request. The Baciguent suppliers may include Baciguent API manufacturers, exporters, distributors and traders.
click here to find a list of Baciguent 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 Baciguent Drug Master File in Japan (Baciguent JDMF) empowers Baciguent 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 Baciguent JDMF during the approval evaluation for pharmaceutical products. At the time of Baciguent 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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