01 1BASF SE
02 1DSM Nutritional Products Ltd.
03 1Zhejiang NHU Company Ltd.
01 1Japanese Pharmacopoeia tocopherol acetate (production only)
02 1Japanese Pharmacopoeia tocopherol acetate ester
03 1Tocopherol acetate VitaminE acetate
01 1China
02 1Germany
03 1Netherlands
Tocopherol acetate (Vitamin E)
Registration Number : 217MF10983
Registrant's Address : Carl-Bosch-Strasse 38,67056 Ludwigshafen, Federal Republic of Germany
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2024-04-03
Japanese Pharmacopoeia Tocopherol Acetate
Registration Number : 219MF10115
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Japanese Pharmacopoeia Tocopherol Acetate (For Manufacturing Use Only)
Registration Number : 224MF10219
Registrant's Address : No. 4 Jiangbeiroad, Yulin street, Xinchang county, Zhejiang province, China
Initial Date of Registration : 2012-11-19
Latest Date of Registration : 2021-05-10
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PharmaCompass offers a list of Vitamin E Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Vitamin E Acetate manufacturer or Vitamin E Acetate supplier for your needs.
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A CCRIS 6054 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCRIS 6054, including repackagers and relabelers. The FDA regulates CCRIS 6054 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCRIS 6054 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 CCRIS 6054 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CCRIS 6054 supplier is an individual or a company that provides CCRIS 6054 active pharmaceutical ingredient (API) or CCRIS 6054 finished formulations upon request. The CCRIS 6054 suppliers may include CCRIS 6054 API manufacturers, exporters, distributors and traders.
click here to find a list of CCRIS 6054 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 CCRIS 6054 Drug Master File in Japan (CCRIS 6054 JDMF) empowers CCRIS 6054 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 CCRIS 6054 JDMF during the approval evaluation for pharmaceutical products. At the time of CCRIS 6054 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 CCRIS 6054 suppliers with JDMF on PharmaCompass.
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