01 1Siegfried PharmaChemikalien Minden GmbH
01 1Isotretinoin
01 1Switzerland
Registration Number : 307MF10079
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2025-07-09
Latest Date of Registration : 2025-07-09
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PharmaCompass offers a list of Isotretinoin 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 Isotretinoin manufacturer or Isotretinoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isotretinoin manufacturer or Isotretinoin supplier.
PharmaCompass also assists you with knowing the Isotretinoin API Price utilized in the formulation of products. Isotretinoin API Price is not always fixed or binding as the Isotretinoin Price is obtained through a variety of data sources. The Isotretinoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ZENATANE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZENATANE, including repackagers and relabelers. The FDA regulates ZENATANE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZENATANE 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 ZENATANE supplier is an individual or a company that provides ZENATANE active pharmaceutical ingredient (API) or ZENATANE finished formulations upon request. The ZENATANE suppliers may include ZENATANE API manufacturers, exporters, distributors and traders.
click here to find a list of ZENATANE 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 ZENATANE Drug Master File in Japan (ZENATANE JDMF) empowers ZENATANE 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 ZENATANE JDMF during the approval evaluation for pharmaceutical products. At the time of ZENATANE 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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