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, 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
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
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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 Aquasol A Parenteral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aquasol A Parenteral, including repackagers and relabelers. The FDA regulates Aquasol A Parenteral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aquasol A Parenteral 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 Aquasol A Parenteral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aquasol A Parenteral supplier is an individual or a company that provides Aquasol A Parenteral active pharmaceutical ingredient (API) or Aquasol A Parenteral finished formulations upon request. The Aquasol A Parenteral suppliers may include Aquasol A Parenteral API manufacturers, exporters, distributors and traders.
click here to find a list of Aquasol A Parenteral suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aquasol A Parenteral CEP of the European Pharmacopoeia monograph is often referred to as a Aquasol A Parenteral Certificate of Suitability (COS). The purpose of a Aquasol A Parenteral CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aquasol A Parenteral EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aquasol A Parenteral to their clients by showing that a Aquasol A Parenteral CEP has been issued for it. The manufacturer submits a Aquasol A Parenteral CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aquasol A Parenteral CEP holder for the record. Additionally, the data presented in the Aquasol A Parenteral CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aquasol A Parenteral DMF.
A Aquasol A Parenteral CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aquasol A Parenteral 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 Aquasol A Parenteral suppliers with CEP (COS) on PharmaCompass.
