01 1BASF SE Ludwigshafen DE
02 2DSM Nutritional Products Ltd. Kaiseraugst CH
01 1Vitamin A concentrate (powder form), synthetic, Palmitate, 250000 IU/g, with all-rac-alpha-tocopherol
02 1Vitamin A, 2.8 MIU/g, acetate
03 1Vitamin A, Not less than 1.7 MIU/g, palmitate
01 1Germany
02 2Netherlands
01 3Valid
Certificate Number : R0-CEP 2019-072 - Rev 00
Status : Valid
Issue Date : 2021-06-21
Type : Chemical
Substance Number : 217
Vitamin A Concentrate (powder Form), Synthetic, ...
Certificate Number : R0-CEP 2021-139 - Rev 00
Status : Valid
Issue Date : 2023-01-11
Type : Chemical
Substance Number : 218
Vitamin A, Not Less Than 1.7 MIU/g, Palmitate
Certificate Number : R1-CEP 2004-301 - Rev 01
Status : Valid
Issue Date : 2021-09-10
Type : Chemical
Substance Number : 217
90
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 ATAV manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ATAV, including repackagers and relabelers. The FDA regulates ATAV manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ATAV 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 ATAV manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ATAV supplier is an individual or a company that provides ATAV active pharmaceutical ingredient (API) or ATAV finished formulations upon request. The ATAV suppliers may include ATAV API manufacturers, exporters, distributors and traders.
click here to find a list of ATAV suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ATAV CEP of the European Pharmacopoeia monograph is often referred to as a ATAV Certificate of Suitability (COS). The purpose of a ATAV CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ATAV EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ATAV to their clients by showing that a ATAV CEP has been issued for it. The manufacturer submits a ATAV CEP (COS) as part of the market authorization procedure, and it takes on the role of a ATAV CEP holder for the record. Additionally, the data presented in the ATAV CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ATAV DMF.
A ATAV CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ATAV CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of ATAV suppliers with CEP (COS) on PharmaCompass.
