01 1DSM Nutritional Products Ltd.
02 1DSM Nutritional Products Ltd.
03 3Riken Vitamin Co., Ltd.
01 1Japanese Pharmacopoeia Retinol palmitate ester (BHA / BHT added)
02 2Japanese Pharmacopoeia retinol palmitate
03 1RIKEN A palmitate 1700
04 1Retinol palmitate Vitamin A Palmitate 1.7m. I. U. / G (with BHA / BHT)
01 3Japan
02 2Netherlands
Japanese Pharmacopoeia Retinol Palmitate
Registration Number : 222MF10268
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2010-12-10
Latest Date of Registration : 2010-12-10
Registration Number : 229MF10223
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2017-12-25
Latest Date of Registration : 2017-12-25
Japanese Pharmacopoeia Retinol Palmitate
Registration Number : 217MF10450
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-24
Latest Date of Registration : 2009-08-07
Japanese Pharmacopoeia Retinol Palmitate (with BHA/BHT)
Registration Number : 219MF10114
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2007-03-23
Retinol palmitate Vitamin A Palmitate 1.7 m. I. U. /g (with BHA/BHT)
Registration Number : 218MF10103
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2006-06-09
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PharmaCompass offers a list of Vitamin A Palmitate 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 Palmitate manufacturer or Vitamin A Palmitate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A Palmitate manufacturer or Vitamin A Palmitate supplier.
PharmaCompass also assists you with knowing the Vitamin A Palmitate API Price utilized in the formulation of products. Vitamin A Palmitate API Price is not always fixed or binding as the Vitamin A Palmitate Price is obtained through a variety of data sources. The Vitamin A Palmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutavit A 500 Plus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutavit A 500 Plus, including repackagers and relabelers. The FDA regulates Lutavit A 500 Plus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutavit A 500 Plus 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 Lutavit A 500 Plus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutavit A 500 Plus supplier is an individual or a company that provides Lutavit A 500 Plus active pharmaceutical ingredient (API) or Lutavit A 500 Plus finished formulations upon request. The Lutavit A 500 Plus suppliers may include Lutavit A 500 Plus API manufacturers, exporters, distributors and traders.
click here to find a list of Lutavit A 500 Plus 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 Lutavit A 500 Plus Drug Master File in Japan (Lutavit A 500 Plus JDMF) empowers Lutavit A 500 Plus 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 Lutavit A 500 Plus JDMF during the approval evaluation for pharmaceutical products. At the time of Lutavit A 500 Plus 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 Lutavit A 500 Plus suppliers with JDMF on PharmaCompass.
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