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01 1Siegfried PharmaChemikalien Minden GmbH
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01 1Oxymetazoline hydrochloride
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01 1Switzerland
Registration Number : 220MF10107
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2008-04-11
Latest Date of Registration : 2024-02-21
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PharmaCompass also assists you with knowing the Oxymetazoline Hydrochloride API Price utilized in the formulation of products. Oxymetazoline Hydrochloride API Price is not always fixed or binding as the Oxymetazoline Hydrochloride Price is obtained through a variety of data sources. The Oxymetazoline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Benzedrex Nasal Spray 12 Hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzedrex Nasal Spray 12 Hour, including repackagers and relabelers. The FDA regulates Benzedrex Nasal Spray 12 Hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzedrex Nasal Spray 12 Hour 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 Benzedrex Nasal Spray 12 Hour manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benzedrex Nasal Spray 12 Hour supplier is an individual or a company that provides Benzedrex Nasal Spray 12 Hour active pharmaceutical ingredient (API) or Benzedrex Nasal Spray 12 Hour finished formulations upon request. The Benzedrex Nasal Spray 12 Hour suppliers may include Benzedrex Nasal Spray 12 Hour API manufacturers, exporters, distributors and traders.
click here to find a list of Benzedrex Nasal Spray 12 Hour 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 Benzedrex Nasal Spray 12 Hour Drug Master File in Japan (Benzedrex Nasal Spray 12 Hour JDMF) empowers Benzedrex Nasal Spray 12 Hour 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 Benzedrex Nasal Spray 12 Hour JDMF during the approval evaluation for pharmaceutical products. At the time of Benzedrex Nasal Spray 12 Hour 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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