01 2DSM Nutritional Products Ltd.
02 1DSM Nutritional Products Ltd. Branch Site Sisseln
01 1Japanese Pharmacopoeia vitamin A oil (BHA / BHT added)
02 1Vitamin A oil Vitamin A Oil
03 1Vitamin A oil Vitamin A Palmitate 1.0m. I. U. / G (wi th Tocopherol)
01 3Netherlands
Japanese Pharmacopoeia Vitamin A Oil (with BHA/BHT)
Registration Number : 219MF10121
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Registration Number : 217MF11120
Registrant's Address : Hauptstrasse 4, CH-4334 Sisseln, Switzerland
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2006-06-09
Vitamin A Oil Vitamin A Palmitate 1.0 m. I. U./g (with tocopherol)
Registration Number : 218MF10107
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2006-03-27
Latest Date of Registration : 2006-05-18
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PharmaCompass offers a list of Vitamin A 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 Vitamin A manufacturer or Vitamin A supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A manufacturer or Vitamin A supplier.
PharmaCompass also assists you with knowing the Vitamin A API Price utilized in the formulation of products. Vitamin A API Price is not always fixed or binding as the Vitamin A Price is obtained through a variety of data sources. The Vitamin A Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rovimix A 500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rovimix A 500, including repackagers and relabelers. The FDA regulates Rovimix A 500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rovimix A 500 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 Rovimix A 500 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rovimix A 500 supplier is an individual or a company that provides Rovimix A 500 active pharmaceutical ingredient (API) or Rovimix A 500 finished formulations upon request. The Rovimix A 500 suppliers may include Rovimix A 500 API manufacturers, exporters, distributors and traders.
click here to find a list of Rovimix A 500 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 Rovimix A 500 Drug Master File in Japan (Rovimix A 500 JDMF) empowers Rovimix A 500 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 Rovimix A 500 JDMF during the approval evaluation for pharmaceutical products. At the time of Rovimix A 500 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Rovimix A 500 suppliers with JDMF on PharmaCompass.
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