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 : 2024-02-21
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxymetazoline Hydrochloride manufacturer or Oxymetazoline Hydrochloride supplier.
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 Neo-Synephrine 12 Hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neo-Synephrine 12 Hour, including repackagers and relabelers. The FDA regulates Neo-Synephrine 12 Hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neo-Synephrine 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.
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A Neo-Synephrine 12 Hour supplier is an individual or a company that provides Neo-Synephrine 12 Hour active pharmaceutical ingredient (API) or Neo-Synephrine 12 Hour finished formulations upon request. The Neo-Synephrine 12 Hour suppliers may include Neo-Synephrine 12 Hour API manufacturers, exporters, distributors and traders.
click here to find a list of Neo-Synephrine 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 Neo-Synephrine 12 Hour Drug Master File in Japan (Neo-Synephrine 12 Hour JDMF) empowers Neo-Synephrine 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 Neo-Synephrine 12 Hour JDMF during the approval evaluation for pharmaceutical products. At the time of Neo-Synephrine 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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