01 1BASF SE Ludwigshafen DE
02 2DSM-FIRMENICH SWITZERLAND AG Kaiseraugst CH
01 1Vitamin A concentrate (powder form), synthetic, Palmitate, 250000 IU/g, with all-rac-α-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 : CEP 2021-139 - Rev 01
Status : Valid
Issue Date : 2025-07-16
Type : Chemical
Substance Number : 218
Vitamin A, Not Less Than 1.7 MIU/g, Palmitate
Certificate Number : CEP 2004-301 - Rev 02
Status : Valid
Issue Date : 2025-07-18
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 Aquasynth manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aquasynth, including repackagers and relabelers. The FDA regulates Aquasynth manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aquasynth 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 Aquasynth manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aquasynth supplier is an individual or a company that provides Aquasynth active pharmaceutical ingredient (API) or Aquasynth finished formulations upon request. The Aquasynth suppliers may include Aquasynth API manufacturers, exporters, distributors and traders.
click here to find a list of Aquasynth suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aquasynth CEP of the European Pharmacopoeia monograph is often referred to as a Aquasynth Certificate of Suitability (COS). The purpose of a Aquasynth CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aquasynth EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aquasynth to their clients by showing that a Aquasynth CEP has been issued for it. The manufacturer submits a Aquasynth CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aquasynth CEP holder for the record. Additionally, the data presented in the Aquasynth CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aquasynth DMF.
A Aquasynth CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aquasynth 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 Aquasynth suppliers with CEP (COS) on PharmaCompass.
