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
A VITAMINA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VITAMINA, including repackagers and relabelers. The FDA regulates VITAMINA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VITAMINA 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 VITAMINA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VITAMINA supplier is an individual or a company that provides VITAMINA active pharmaceutical ingredient (API) or VITAMINA finished formulations upon request. The VITAMINA suppliers may include VITAMINA API manufacturers, exporters, distributors and traders.
click here to find a list of VITAMINA 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 VITAMINA Drug Master File in Japan (VITAMINA JDMF) empowers VITAMINA 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 VITAMINA JDMF during the approval evaluation for pharmaceutical products. At the time of VITAMINA 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 VITAMINA suppliers with JDMF on PharmaCompass.
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