01 2DSM Nutritional Products Ltd.
01 1Dry Vitamin A Acetate, type 500 Dry Vitamin A Ace tate 500
02 1Dry vitamin A acetate, type 500B Dry Vitamin A A cetate 500B①
01 2Netherlands
Dry Vitamin A Acetate, Type 500B Dry Vitamin A Acetate 500B①
Registration Number : 224MF10063
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2012-04-01
Latest Date of Registration : 2012-04-01
Dry Vitamin A Acetate, Type 500
Registration Number : 218MF10553
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2007-09-18
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PharmaCompass offers a list of Vitamin A Acetate 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 Acetate manufacturer or Vitamin A Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A Acetate manufacturer or Vitamin A Acetate supplier.
PharmaCompass also assists you with knowing the Vitamin A Acetate API Price utilized in the formulation of products. Vitamin A Acetate API Price is not always fixed or binding as the Vitamin A Acetate Price is obtained through a variety of data sources. The Vitamin A Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EC 204-844-2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EC 204-844-2, including repackagers and relabelers. The FDA regulates EC 204-844-2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EC 204-844-2 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 EC 204-844-2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EC 204-844-2 supplier is an individual or a company that provides EC 204-844-2 active pharmaceutical ingredient (API) or EC 204-844-2 finished formulations upon request. The EC 204-844-2 suppliers may include EC 204-844-2 API manufacturers, exporters, distributors and traders.
click here to find a list of EC 204-844-2 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 EC 204-844-2 Drug Master File in Japan (EC 204-844-2 JDMF) empowers EC 204-844-2 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 EC 204-844-2 JDMF during the approval evaluation for pharmaceutical products. At the time of EC 204-844-2 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 EC 204-844-2 suppliers with JDMF on PharmaCompass.
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