01 1Siegfried PharmaChemikalien Minden GmbH
01 1Oxymetazoline hydrochloride
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 : 2025-10-29
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PharmaCompass offers a list of Oxymetazoline Hydrochloride 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 Oxymetazoline Hydrochloride manufacturer or Oxymetazoline Hydrochloride supplier for your needs.
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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 Nasivin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nasivin, including repackagers and relabelers. The FDA regulates Nasivin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nasivin 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 Nasivin supplier is an individual or a company that provides Nasivin active pharmaceutical ingredient (API) or Nasivin finished formulations upon request. The Nasivin suppliers may include Nasivin API manufacturers, exporters, distributors and traders.
click here to find a list of Nasivin 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 Nasivin Drug Master File in Japan (Nasivin JDMF) empowers Nasivin 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 Nasivin JDMF during the approval evaluation for pharmaceutical products. At the time of Nasivin 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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